front 1 What covalent change occurs in Na+/K+-ATPase
when K+ is transported into the cell? | back 1 dephosphorylated |
front 2 The ATP binding site of Na+/K+-ATPase is located on which side of the plasma membrane? | back 2 Cytosolic side |
front 3 What is the mechanism of action of cardiac glycosides? | back 3 Na+/K+-ATPase blockade → Decreased activity of Na+/Ca2+ antiporter → Increased [Ca2+] intracellularly → Increase in cardiac contractility |
front 4 For each ATP consumed, Na+/K+-ATPase transports
how many Na+ and K+ molecules, and in what
direction? | back 4 3 Na+ molecules out |
front 5 What two cell types are rich in the smooth endoplasmic
reticulum? | back 5 Steroid hormone-producing cells |
front 6 Which organelle is resposible for steroid synthesis and detoxification of poisons and drugs? | back 6 Smooth endoplasmic reticulum |
front 7 Which organelle found in the rough endoplasmic reticulum is missing from the smooth endoplasmic reticulum? | back 7 Surface ribosomes |
front 8 Name the enzyme involved in both glycogenolysis and gluconeogenesis that is found in the smooth endoplasmic reticulum. | back 8 Glucose-6-phosphatase |
front 9 Where are cytosolic, peroxisomal, and mitochondrial proteins synthesized? | back 9 Free ribosomes |
front 10 What is the histologic term for the rough endoplasmic reticulum in neurons? | back 10 Nissl bodies |
front 11 Name two cell types that would be rich in the rough endoplasmic reticulum. | back 11 Goblet cells |
front 12 Which organelle synthesizes secretory proteins and adds N-linked oligosaccharides to proteins? | back 12 Rough endoplasmic reticulum |
front 13 Defects in the ubiquitin-proteasome system have been linked to which
neurologic disease? | back 13 Parkinson disease |
front 14 Which barrel-shaped protein complex degrades damaged or ubiquitin-tagged proteins? | back 14 Proteasome |
front 15 What screening test can be used to identify patients with primary ciliary dyskinesia? | back 15 Nasal nitric oxide |
front 16 Nasal nitric oxide would be _____ in primary ciliary dyskinesia | back 16 decreased |
front 17 Where are proteins within Golgi bodies, lysosomes, and the endoplasmic reticulum synthesized? | back 17 Rough endoplasmic reticulum |
front 18 Why would a patient with the finding in the chest X-ray shown be at an increased risk for hearing loss? [...] of the [...] is dysfunctional | back 18 Cilia of the eustachian tube is dysfunctional |
front 19 Why are patients with primary ciliary dyskinesia likely to be
infertile or develop recurrent ectopic pregnancy? | back 19 Dysfunctional cilia of the fallopian tube in females |
front 20 What leads to dysfunctional cilia in patients with primary ciliary
dyskinesia? | back 20 dynein arm |
front 21 Why do patients with primary ciliary dyskinesia develop recurrent
infections of the respiratory tract? | back 21 mucociliary clearance |
front 22 What is the mode of inheritance of primary ciliary dyskinesia? | back 22 Autosomal recessive |
front 23 What is this? | back 23 osteogenesis imperfecta |
front 24 What is the pathophysiology of a disease in a child with poor dentition, blue sclerae, and fractures and bone deformities after minimal trauma? Decreased production of ______ ______ ______ | back 24 Decreased production of type I collagen |
front 25 What medication can help reduce the incidence of fractures in patients with osteogenesis imperfecta? ______ | back 25 Bisphosphonates |
front 26 What is the pathophysiology behind opalescent teeth in patients with
osteogenesis imperfecta? | back 26 dentin |
front 27 How is the most common form of osteogenesis imperfecta inherited? | back 27 Autosomal dominant |
front 28 What is the cause of conductive hearing loss in a child with recurrent fractures and blue sclerae as shown in the image below? ______ ______ | back 28 Abnormal ossicles |
front 29 What are the manifestations of osteogenesis imperfecta? | back 29 Multiple fractures |
front 30 What are the most common genetic mutations involved in osteogenesis imperfecta? ______ ______ | back 30
COL1A1 |
front 31 What causes blue sclerae in osteogenesis imperfecta? ______ connective tissue overlying ______ veins | back 31 Translucent, choroidal |
front 32 Which type of collagen is affected in the vascular type of Ehlers-Danlos syndrome? ______ ______ ______ | back 32 Type III collagen |
front 33 What is the most common type of Ehlers-Danlos syndrome? ______ type | back 33 Hypermobility type |
front 34 Ehlers-Danlos syndrome is transmitted through what two inheritance patterns? ______ ______ ______ ______ | back 34 Autosomal dominant |
front 35 Ehlers-Danlos syndrome is due to a defect in what process? ______ ______ | back 35 Collagen synthesis |
front 36 What types of aneurysms are commonly associated with Ehlers-Danlos
syndrome? | back 36 Berry aneurysms |
front 37 What type of specific collagen is affected in a patient with easy bruising and findings as shown in the image below? | back 37 Type V collagen |
front 38 Which type of Ehlers-Danlos syndrome has fragile vessels, muscles, and organs prone to rupture? ______ ______. There is a mutation in type III collagen caused by ______. | back 38 Vascular type COL3A1. |
front 39 What is this? | back 39 Cilia |
front 40 Cilia consist of microtubules arranged in ___ doublets around ___ central singlets. | back 40 9 2 |
front 41 Which cellular structure is shown in the image below? | back 41 Basal body |
front 42 Basal body is located at the ___ of the ___, below the cell membrane. | back 42 base clium |
front 43 Basal Body constists of ___ ___ ___ without any central microtubules. | back 43 9 microtubule triplets |
front 44 What ATPase protein links the peripheral nine doublets and allows for bending of the cilia by differential sliding of the doublets? ___ ___ | back 44 Axonemal dynein |
front 45 What cell junctions allow for coordinated movement of cilia? ___ ___ | back 45 Gap junctions |
front 46 What type of cilia act as chemical signal sensors and play a role in signal transduction and control of cell growth? ___ ___ | back 46 Non-motile cilia |
front 47 Non-motile cilia is AKA ___ cilia. | back 47 primary |
front 48 Which conditions may occur due to dysgenesis of non-motile
cilia? | back 48 Retinal degeneration |
front 49 Common complications of EDS include aortic and berry aneurysms, mitral valve prolapse, and ___ ___. | back 49 organ rupture. |
front 50 What is the most common enzyme deficiency that leads to
homocystinuria? | back 50 Cystathionine synthase deficiency |
front 51 Elastin is rich in which three amino acids? | back 51 Proline |
front 52 What is the function of fibrillin-1? | back 52 elastin tgf-b |
front 53 What enzyme is inhibited by α1-antitrypsin? | back 53 Elastase |
front 54 Elastase degrades [...] | back 54 elastin |
front 55 In which cellular compartment does cross-linking of elastin by lysyl oxidase occur? | back 55 Extracellular space |
front 56 Name two aortic/vascular pathologies associated with Marfan
syndrome. | back 56 Aortic root aneurysm rupture or dissection |
front 57 What is arachnodactyly? | back 57 Long, tapering fingers and toes |
front 58 arachnodactyly is seen in patients with _____ syndrome or _____. | back 58 Marfan homocystinuria |
front 59 What valvular abnormality is most commonly associated with Marfan syndrome? | back 59 Mitral valve prolapse |
front 60 How is lens dislocation in Marfan syndrome different from that in
homocystinuria? | back 60 Lens dislocate upward and temporal in Marfan syndrome |
front 61 How does Marfan syndrome affect the intellect of a patient? homocystinuria? | back 61 Normal Decreased |
front 62 What lung disease can be caused by a deficiency of α1-antitrypsin? | back 62 COPD |
front 63 A mutation in what gene is responsible for a tall child presenting with arachnodactyly, hypermobile joints, and the deformity in the image? A mutation in ____ on chromosome ____ | back 63 FBN1, 15 |
front 64 What is the inheritance pattern of Marfan syndrome? | back 64 Autosomal dominant |
front 65 What protein is abundantly found in the vocal cords, epiglottis, lungs, large arteries, elastic ligaments, skin, and ligamenta flava? | back 65 Elastin |
front 66 Which disease presents with an increased arm to height ratio, pectus deformity, skin hyperelasticity, arachnodactyly, and scoliosis similar to Marfan syndrome? | back 66 Homocystinuria |
front 67 Impaired copper metabolism in Menkes disease ultimately results in a defective production of what protein? | back 67 Collagen |
front 68 What is the diagnosis for a child who has brittle, "kinky" hair, hypotonia, delays in growth and development, and an increased risk for cerebral aneurysms? | back 68 Menkes disease |
front 69 How do serum copper levels differ in Menkes disease when compared
with Wilson disease? | back 69 low high |
front 70 The activity of what enzyme is decreased in Menkes disease? Why? | back 70 Lysyl oxidase Copper is a necessary cofactor |
front 71 Menkes gene? | back 71 ATP7A |
front 72 impairment at which point is responsible for the pathophysiology of Li-Fraumeni syndrome and cervical cancer? modulated by what? | back 72 The G1-S checkpoint p53 |
front 73 What are cyclins? | back 73 Regulatory CDKs growth |
front 74 List the three components of interphase. | back 74 G1 phase |
front 75 Which type of cells divide rapidly with a short G1 phase, never enter G0 phase, and are most affected by chemotherapy? | back 75 Labile cells |
front 76 What cells include hepatocytes, periosteal cells, proximal convuluted tubule cells, and lymphocytes. | back 76 Stable cells |
front 77 What cells include hair follicles, skin, bone marrow, gut epithelium, and germ cells? | back 77 Labile cells |
front 78 What cell type, as classified by cell cycle regulation, can enter the G1 phase of the cell cycle from the G0 phase when stimulated? | back 78 Stable cells |
front 79 Permanent cells such as neurons, red blood cells, skeletal myocytes, and cardiac myocytes are arrested in which phase of the cell cycle? | back 79 G0 phase |
front 80 Which phase of the cell cycle has a variable duration? | back 80 G1 phase |
front 81 Which phase of the cell cycle is usually the shortest? | back 81 M phase |
front 82 During which phase of the cell cycle can a cell enter the G0 phase? | back 82 G1 phase |
front 83 When does DNA synthesis occur in the cell cycle? | back 83 S phase |
front 84 What two processes occur during the M phase? | back 84 Mitosis |
front 85 Mitosis is the splitting of the _______. Cytokinesis is the splitting of the _______. | back 85 nucleus cytoplasm |
front 86 What is the mechanism by which the p53 protein inhibits the
progression of the cell cycle from the G1 phase to the S
phase? | back 86 p21 CDK retinoblastoma |
front 87 How do growth factors promote the transition of a cell from the
G1 phase to the S phase? | back 87 tyrosine kinase |
front 88 What is the result of having a dysfunctional signal recognition
particle in the cell? | back 88 protein |
front 89 Endosomes act as sorting centers for molecules that are destined for
what two purposes? | back 89 degradation further |
front 90 What is the role of COPII in vesicular trafficking? | back 90 anterograde cis |
front 91 Which vesicular protein is involved in the trafficking of molecules taken into the cell via receptor-mediated endocytosis? | back 91 clathrin |
front 92 In the Golgi apparatus, the addition of what carbohydrate to proteins makes them a target for lysosomes? | back 92 Mannose-6-phosphate |
front 93 What is the role of COPI in vesicular trafficking? | back 93 Retrograde cis |
front 94 What is the prognosis for a child with symptoms similar to but more
severe than those of Hurler syndrome, who has elevated plasma
lysosomal enzymes? This is [...] disease. | back 94 fatal inclusion-cell |
front 95 A boy has coarse facial features, gingival hyperplasia, corneal clouding, claw hand, kyphoscoliosis, and high levels of lysosomal enzymes. What is the inheritance pattern? | back 95 Autosomal recessive |
front 96 N-acetylglucosaminyl-1-phosphotransferase problem, what disease. | back 96 inclusion-cell disease |
front 97 What are the three posttranslational modifications that occur in the
Golgi apparatus? | back 97 Modification of N-oligosaccharides on asparagine |
front 98 Clathrin functions to transport vesicles from the trans-Golgi apparatus to which organelle? | back 98 Lysosome |
front 99 List three locations to which the Golgi apparatus sends proteins and lipids. ______ ______ | back 99 Plasma membrane |
front 100 The Golgi apparatus acts as a distribution center for what 2 macromolecules? | back 100 Proteins |
front 101 Which enzyme system mediates phase I metabolism of drugs in the body? | back 101 CYP450 |
front 102 What is the definition of the relapse phase of the transtheoretical model of change? | back 102 Patient falls back to previous behavior |
front 103 What function does the product of TP53 normally
perform? | back 103 p21 g1 s |
front 104 An S3 heart sound is caused by _______ filling pressures in _______ _______ during rapid ventricular filling phase | back 104 increased early diastole |
front 105 What 2 heart murmurs have no true isovolumetric phases? | back 105 Aortic regurgitation Mitral regurgitation |
front 106 Topoisomerase inhibitors used in cancer treatment all cause cell cycle arrest at which two phases? | back 106 S G2 |
front 107 Melanomas have a tumor suppressor gene mutation at CDKN2A. What protein does this gene typically encode? | back 107 p16 |
front 108 Is the corpus luteum present during the follicular or luteal phase of the menstrual cycle? | back 108 luteal phase |
front 109 The corpus luteum is formed from the ruptured _______ and produces _______ . | back 109 follicle progesterone |
front 110 In which phase of the cell cycle does nucleotide excision repair occur? | back 110 G1 |
front 111 In which phase of the cell cycle does mismatch repair occur? | back 111 S |
front 112 In which phase of the cell cycle does base excision repair occur? | back 112 It occurs throughout the cell cycle |
front 113 In which phase of the cell cycle do microtubule inhibitors exert their effects? | back 113 M |
front 114 A first-in-human protocol enrolls healthy volunteers and maps effects
as a function of dose. This is: | back 114 A. Phase 1 trial |
front 115 A study enrolls patients with the target disease to determine whether
the drug is efficacious. This is: | back 115 D. Phase 2 trial |
front 116 A program expands to much larger numbers of target-disease patients
to establish and confirm safety and efficacy. This is: | back 116 B. Phase 3 trial |
front 117 Post-approval monitoring begins only after marketing permission is
obtained. This corresponds to: | back 117 C. Phase 4 |
front 118 What 2 sympathetic chain synapses may be compromised in a patient who has Horner syndrome? | back 118 lateral horn superior cervical ganglion |
front 119 What facial syndrome may occur as a result of spinal cord lesions above T1 or a Pancoast tumor at the stellate ganglion? | back 119 Horner Syndrome |
front 120 horner classic triad | back 120 ptosis anhidrosis miosis |
front 121 A hypoplastic nasal bone and an increase in nuchal translucency is present on a fetal ultrasound exam. What is the diagnosis? | back 121 down syndrome |
front 122 Apart from labor contractions and milk letdown, what role does oxytocin play in mood? | back 122 regulates it |
front 123 Down syndrome is most frequently caused by a defect in what process | back 123 Meiotic nondisjunction |
front 124 Females of which age group are at an increased risk of having a child
with Down syndrome? | back 124 advanced |
front 125 Glucagon stimulates the breakdown of glycogen by which second-messenger system? | back 125 cAMP |
front 126 Is the promoter region upstream or downstream of its gene locus? | back 126 Upstream |
front 127 Lactase breaks down lactose into which two monosaccharides? | back 127 Galactose Glucose |
front 128 Rank the incidence of the three most common trisomy disorders. ____ syndrome > ____ syndrome > ____ syndrome | back 128 Down syndrome > Edwards syndrome > Patau syndrome |
front 129 What are two functions of oxytocin in the perinatal period? | back 129 letdown contraction |
front 130 What could cause a person to always use more drugs than intended despite knowing the dangers and trying to cut down on use? | back 130 substance use disorder |
front 131 What disease is suspected if a newborn with evidence of Down syndrome on prenatal screening does not pass meconium after birth but is not vomiting? | back 131 Hirschsprung disease |
front 132 What is the likely cause of sharp, shooting pains that travel down the jaw for several seconds when eating ice cream? | back 132 Trigeminal neuralgia |
front 133 What is the name of the phenomenon by which alleles that increase a species' fitness are more likely to be passed down to offspring? | back 133 natural selection |
front 134 What ophthalmologic finding may be present in a patient with Down syndrome? | back 134 Brushfield spots |
front 135 What organ does glucagon act on to stimulate the breakdown of glycogen? | back 135 Liver |
front 136 What type of hernia is commonly seen in patients with Down syndrome? | back 136 umbilical hernia |
front 137 Which DNA mutation results from an insertion or a deletion of nucleotides that is not divisible by three? | back 137 Frameshift mutation |
front 138 Which enzyme of DNA replication is often upregulated in progenitor cells and tumor cells and downregulated in aging and progeria? | back 138 Telomerase |
front 139 what is this? | back 139 duodenal atresia |
front 140 While breastfeeding, which hormone causes milk letdown in a mother? | back 140 Oxytocin |
front 141 Why are patients with Down syndrome at higher risk of developing Alzheimer disease? _____ is located on chromosome _____ | back 141 APP is located on chromosome 21 |
front 142 Mutations of amyloid precursor protein can lead to early-onset _____ _____ . | back 142 Alzheimer disease |
front 143 down syndrome has low levels of what protein? | back 143 α-fetoprotein |
front 144 What is the Wolff-Chaikoff effect? _____ of the thyroid gland in response to _____ iodine levels | back 144 Downregulation of the thyroid gland in response to high iodine levels |
front 145 What is the most common heritable cause of intellectual disability? | back 145 fragile x syndrome |
front 146 most common cause of genetic intellectual disability? | back 146 down syndrome |
front 147 What is the major difference between necrosis and apoptosis? | back 147 inflammation membrane |
front 148 Duplication of which chromosome results in Klinefelter syndrome? | back 148 Chromosome X |
front 149 Testicular atrophy and infertility in a tall male patient with eunuchoid proportions may indicate which disorder of sex chromosomes? | back 149 Klinefelter |
front 150 A Barr body is an _____ _____ chromosome; found in _____ syndrome in males | back 150 inactivated X Klinefelter |
front 151 What will an ovarian biopsy show in a patient with Turner syndrome? ____ ____ AKA ____ ____ | back 151 ovarian dysgenesis AKA streak ovary |
front 152 Why are females with Turner syndrome more likely to have an X-linked
recessive disorder? | back 152 X |
front 153 How many Barr bodies are seen when the cells of a patient with Turner syndrome are examined under the microscope? | back 153 0 |
front 154 In patients with Turner syndrome due to a meiosis error, in which gamete does the error typically occur? | back 154 paternal |
front 155 Patients with ______ are less likely to develop hypertension than those with pheochromocytoma. | back 155 neuroblastoma |
front 156 What will be elevated on urine and blood analysis of a patient with
pheochromocytoma? | back 156 catecholamines metanephrines |
front 157 When managing a pheochromocytoma, why must administration of an α-antagonist precede administration of a β-blocker and surgical resection? To prevent ______ ______ | back 157 hypertensive crisis |
front 158 Which drug should be given preoperatively for resection of a pheochromocytoma? ______ | back 158 Phenoxybenzamine |
front 159 Why should β-blockers be used with caution in the treatment of
pheochromocytoma and in patients who have recently used cocaine? | back 159 α1 |
front 160 Opioid use can result in depression of which 2 organ systems? | back 160 CNS Respiratory System |
front 161 The following symptoms may be present in a patient with withdrawal
from which psychoactive drug? | back 161 Cocaine |
front 162 What two symptoms can be present with benzodiazepine intoxication? ______ depression ______ | back 162 respiratory depression ataxia |
front 163 Which anesthetic class can cause malignant hyperthermia, myocardial depression, and a decrease in cerebral metabolic demand? ______ ______ | back 163 Inhaled anesthetics |
front 164 Which drug class is indicated in the treatment of depression and generalized anxiety disorder and can also be used for diabetic neuropathy? | back 164 SNRIs |
front 165 Why are barbiturates contraindicated for patients with a history of alcohol use disorder? They have an additive _____ depression effect when combined with alcohol | back 165 CNS |
front 166 Trazodone causes _____, which is desirable in the treatment of insomnia | back 166 sedation |
front 167 What psychiatric disorder should be ruled out before a diagnosis of dementia is made? | back 167 Depression |
front 168 What is the most common subtype of depression? | back 168 Depression with atypical features |
front 169 What is the likely diagnosis for an adult with a history of chronic alcohol consumption who is exhibiting anterograde amnesia and confabulation in the emergency department? ______ syndrome | back 169 Korsakoff syndrome |
front 170 What type of amnesia is present in a patient who sustained a head injury and is unable to recall anything that occurred from the time that the injury occurred? ______ amnesia | back 170 Anterograde amnesia |
front 171 What motor protein is responsible for anterograde transport of cargo on microtubules? | back 171 Kinesin |
front 172 HSV, poliovirus, and rabies virus use which molecular motor protein for retrograde transport to reach the cell body? | back 172 Dynein |
front 173 What molecular defect is responsible for dextrocardia, as seen in Kartagener syndrome? A defect in _____ | back 173 dynein |
front 174 One-third of collagen is composed of which amino acid? | back 174 Glycine |
front 175 What cofactor is required for the hydroxylation of proline and lysine residues in collagen? | back 175 vitamin C |
front 176 What two amino acids undergo hydroxylation in collagen synthesis? | back 176 proline, lysine |
front 177 Which two genetic diseases are associated with bronchiectasis? _____ _____ _____ syndrome | back 177 Cystic fibrosis Karragener |
front 178 Cystic fibrosis, Kartagener both impair lung clearance of _____. | back 178 pathogens |
front 179 What two conditions classically impair ciliary motility and may lead to bronchiectasis? chronic _____ _____ syndrome | back 179 chronic smoking kartagener syndrome |
front 180 What is the mode of inheritance of Kartagener syndrome? _____ _____ | back 180 Autosomal recessive |
front 181 what is this? | back 181 fetal alcohol syndrome |
front 182 What limb abnormality is associated with fetal alcohol syndrome? | back 182 dislocation |
front 183 A child is diagnosed with autism. When does this disorder present, and is it more common in girls or boys? Autism must present in _____ childhood and is more common in _____ | back 183 early boys |
front 184 A child is unable to read near the level of proficiency for his or her age even after working with a tutor 7 months. What is the most likely diagnosis? _____ _____ disorder | back 184 specific learning disorder |
front 185 An episode of separation anxiety in older children must last how long for it to be considered a disorder? _____ _____ or more | back 185 4 weeks |
front 186 At what age can you diagnose a patient with conduct disorder? | back 186 before 18 |
front 187 What is intellectual disability? _____ cognitive deficits that affect memory, reasoning, judgment, abstract thinking, language, and learning | back 187 Global |
front 188 What term describes weight loss, muscle atrophy, and fatigue in the setting of chronic or terminal illness? | back 188 Cachexia |
front 189 In which direction will the tongue deviate with a lesion of the right hypoglossal nerve? | back 189 right |
front 190 Lesion in which cranial nerve may cause weakness in shrugging the shoulder? | back 190 cranial nerve 11 |
front 191 Lesion in which cranial nerve, and on what side, may deviate the uvula to the right? | back 191 left, cn X |
front 192 Lesion of which cranial nerve, and on what side, may deviate the jaw to the right? | back 192 right, cn V |
front 193 cn v injury: The jaw deviates toward the same side as the lesion due to unopposed force from the opposite _____ muscle. | back 193 pterygoid |
front 194 The sternocleidomastoid muscle is innervated by the spinal _____ nerve and turns the head to the _____ side. | back 194 accessory contralateral |
front 195 Dysfunction of what anatomical structure is associated with increased risk of developing otitis media? _____ _____ | back 195 Eustachian tube |
front 196 What complication presenting with erythema and swelling of the postauricular region might arise after an unresolved acute otitis media infection? _____ | back 196 Mastoiditis |
front 197 What is a dreaded complication of mastoiditis? _____ _____ | back 197 Brain abscess |
front 198 What is the most common pathogen associated with otitis externa? _____ | back 198 Pseudomonas |
front 199 What pathology of the ear is associated with water exposure, occlusion, and trauma of the ear canal? | back 199 Otitis externa |
front 200 Otitis externa AKA _____ _____ | back 200 swimmer's ear |
front 201 What metabolic pathway is affected in alkaptonuria? Degradation of _____ to _____ | back 201 tyrosine fumarate |
front 202 What is the inheritance pattern of alkaptonuria? | back 202 Autosomal recessive |
front 203 What causes joint pain in a patient with alkaptonuria? Buildup of _____ _____. This is toxic to _____. | back 203 homogentisic acid cartilage |
front 204 Which benign enzyme deficiency causes arthralgias, darkened sclerae and connective tissues, and urine that turns black on air exposure? _____ _____ deficiency | back 204 Homogentisate oxidase deficiency |
front 205 What biochemical anomaly explains reduced blood pressure in a patient
with scurvy? | back 205 collagen C |
front 206 Vitamin C is required to convert dopamine to _____. | back 206 norepinephrine |
front 207 NAD+ and NADP+ are derived from which amino acid? | back 207 Tryptophan |
front 208 Which amino acid and vitamin produces histamine? | back 208 Histidine |
front 209 What amino acid and cofactor are required to produce porphyrin, the precursor to heme? | back 209 Glycine |
front 210 What amino acid can be used to synthesize creatinine, urea, and nitric oxide? | back 210 Arginine |
front 211 The conversions of phenylalanine to tyrosine and tyrosine to dopa require what cofactor? | back 211 BH4 |
front 212 Thyroxine is derived from which amino acid? | back 212 Tyrosine |
front 213 Melanin is derived from which compound? | back 213 Dopa |
front 214 The conversion of dopa to dopamine requires what cofactor? | back 214 Vitamin B6 |
front 215 Norepinephrine is converted into epinephrine via a methyl group provided by what cofactor? | back 215 S-adenosylmethionine |
front 216 What two cofactors are needed to produce NAD+ and
NADP+ from tryptophan? | back 216 Vitamin B2 |
front 217 What two cofactors are needed to produce melatonin from tryptophan? | back 217 BH4 |
front 218 What neurotransmitter is produced from glutamate? Mention the required cofactor. | back 218 GABA |
front 219 What is the final common target of the intrinsic and extrinsic
pathways of apoptosis? | back 219 caspases |
front 220 What two seperate mechanisms trigger the extrinsic apoptotic
pathway? | back 220 Ligand-receptor interactions |
front 221 What happens to apoptotic bodies after they are formed? | back 221 phagocytosed |
front 222 There are no ______ ______ to electroconvulsive therapy. | back 222 absolute contraindications |
front 223 Name four clinical indications for electroconvulsive therapy. | back 223 Acute suicidality |
front 224 What is the mechanism of electroconvulsive therapy? | back 224 tonic-clonic |
front 225 What are the adverse effects of electroconvulsive therapy? | back 225 Headache |
front 226 What kind of medical care aims at improving quality of life in patients with serious illnesses despite their prognosis and is often given with curative treatment? | back 226 Palliative care |
front 227 What should be the life expectancy of the patients to be eligible for
hospice care? | back 227 6 months |
front 228 Which type of medical care focuses on providing comfort and
palliation instead of a definitive cure in patients with a prognosis
of < 6 months? | back 228 Hospice care |
front 229 What intracellular proteins are responsible for facilitating and
maintaining protein folding? | back 229 Chaperone proteins |
front 230 Name the special class of chaperone proteins that prevents protein
denaturation at high temperatures in yeast. | back 230 Heat shock proteins |
front 231 Which part of Medicare provides prescribed drugs? | back 231 Part D |
front 232 Medicare is available to what group of patients? | back 232 Patients ≥ 65 years old |
front 233 What are the two federal social healthcare programs that originated from amendments to the Social Security Act? | back 233 Medicare |
front 234 What services do part A of Medicare give? | back 234 Hospital admissions |
front 235 What services does part B of Medicare provide? | back 235 Basic medical bills |
front 236 What services does part C of Medicare provide? | back 236 Hospital admissions |
front 237 The yellow-brown pigments, called _______, are due to lipid _______ of polyunsaturated lipids of subcellular membranes | back 237 lipofuscin peroxidation |
front 238 lipofuscin pigments in various organs is part of the normal ______ process | back 238 aging |
front 239 What is lipofuscin composed of? | back 239 Polymers of lipids and phospholipids complexed with protein |
front 240 How is polycythemia further subtyped? | back 240 Relative |
front 241 What changes in red blood cell mass, O2 saturation, and erythropoietin levels do you expect in polycythemia vera? [...] O2 saturation [...] red blood cell mass [...] erythropoietin levels | back 241 ↓ O2 saturation |
front 242 What levels of red blood cell mass, O2 saturation, and
erythropoietin would be expected in a patient with relative
polycythemia? | back 242 Normal red blood cell mass |
front 243 What changes in red blood cell mass, O2 saturation, and
erythropoietin levels do you expect in appropriate absolute causes of
polycythemia? | back 243 Dec O2 saturation |
front 244 What changes in red blood cell mass, O2 saturation, and
erythropoietin levels do you expect in inappropriate absolute causes
of polycythemia? | back 244 Normal O2 saturation |
front 245 How are plasma volume levels affected in absolute polycythemia? | back 245 Normal plasma volume levels |
front 246 In what two conditions do you expect to see inappropriate absolute
polycythemia? | back 246 Exogenous erythropoietin administration from athlete
abuse |
front 247 In what three conditions may appropriate absolute polycythemia be
seen? | back 247 High altitude |
front 248 In what conditions are relative polycythemia imminent? | back 248 burns dehydration |
front 249 Barrett esophagus leads to increased risk of what cancer? | back 249 Adenocarcinoma |
front 250 Where is a drug with small lipophilic molecules typically distributed? | back 250 Tissues |
front 251 What cardiovascular changes occur on the left side cavities of the
heart due to normal aging? | back 251 Decrease in the size of the left ventricular cavity |
front 252 What effect does immunosenescence due to normal aging have on
immunity? | back 252 Decreases |
front 253 What changes due to normal aging occur with arterial compliance,
aortic diameter, heart rate, and the aortic and mitral valves? | back 253 Decrease in arterial compliance |
front 254 Name three gastrointestinal changes that occur due to normal
aging. | back 254 Decrease in lower esophageal sphincter tone |
front 255 What two changes occur in bone marrow due to normal aging? | back 255 Decrease in bone marrow mass |
front 256 What effect does normal aging have on adaptive immunity? | back 256 Decrease in naive B cells and T cells |
front 257 Name three musculoskeletal changes that occur due to normal
aging. | back 257 Decrease in skeletal muscle mass |
front 258 What two nervous system changes occur due to normal aging? | back 258 Decrease in brain volume |
front 259 Name five skin changes that occur due to normal aging. | back 259 Atrophy and flattening of dermal-epidermal junction |
front 260 What is a cause of chronological or intrinsic aging of the
skin? | back 260 Decreased synthesis capacity of dermal fibroblasts |
front 261 How does sun exposure contribute to aging? | back 261 Ultraviolet rays degrade dermal collagen and elastin |
front 262 Name three renal changes that occur due to normal aging. | back 262 Decrease in glomerular filtration rate |
front 263 How does aging alter the male reproductive system? | back 263 Testicular atrophy |
front 264 Name five vaginal changes that occur due to normal aging. | back 264 Vulvovaginal atrophy |
front 265 How does aging affect libido? | back 265 decreases |
front 266 How does aging alter lung and chest wall compliance? | back 266 Increases lung compliance |
front 267 How does aging alter residual lung volume, V/Q mismatch, and the A-a
gradient? | back 267 Increases residual lung volume |
front 268 How does aging alter FEV1, FVC, and respiratory muscle
strength? | back 268 Decreases FEV1 |
front 269 How does total lung capacity change during normal aging? | back 269 no change! |
front 270 How does aging affect ventilatory response to
hypoxia/hypercapnia? | back 270 Decreased |
front 271 How does aging affect lung mucus clearance? | back 271 Slower mucociliary clearance |
front 272 What is this? ____ It presents with a high bacterial ____ and low cell-mediated ____. | back 272 leprosy load immunity |
front 273 Which animals serve as reservoirs of Mycobacterium leprae in the United States? | back 273 Aramadillos |
front 274 Which form of leprosy presents with hypoesthetic, hairless skin
nodules? | back 274 Tuberculoid leprosy |
front 275 Which form of leprosy presents with diffuse, communicable skin
lesions and leonine facies? | back 275 Lepromatous leprosy |
front 276 How do you confirm a Mycobacterium leprae infection? | back 276 Tissue PCR |
front 277 Compare T-cell responses associated with lepromatous leprosy and
tuberculoid leprosy. | back 277 Lepromatous leprosy causes a Th2 response |
front 278 Infection with which mycobacterium leads to a "glove and stocking" loss of sensation? | back 278 Mycobacterium leprae |
front 279 What type of collagen is defective in Alport syndrome? | back 279 Type IV collagen |
front 280 What type of collagen is targeted by autoantibodies in Goodpasture
syndrome? | back 280 Type IV collagen |
front 281 Name the most abundant protein in the body, which undergoes extensive
posttranslational modification. | back 281 Collagen |
front 282 Which type of collagen makes up reticulin? | back 282 Type III collagen |
front 283 What cells are responsible for secretion of type IV collagen and
wound contraction? | back 283 Myofibroblasts |
front 284 In what structures can type IV collagen be found? | back 284 Basement membrane |
front 285 What structures are composed of type II collagen? | back 285 Cartilage pulposus body |
front 286 What is going on? Replacement of [keratinized/nonkeratinized] [simple/stratified] squamous epithelium with [ciliated/nonciliated] [simple/cuboidal/columnar] epithelium with [...] cells | back 286 Replacement of nonkeratinized stratified squamous epithelium with nonciliated columnar epithelium with goblet cells |
front 287 A patient with chronic reflux esophagitis undergoes a workup. Findings on endoscopy are shown. What is the diagnosis? | back 287 Barrett esophagus |
front 288 Barrett esophagus is an example of what kind of pathologic aberration to the normal tissue histology? | back 288 Metaplasia |
front 289 What do the inclusion bodies indicated by the arrow in the image, often seen in those with alcoholic hepatitis, represent? | back 289 Mallory bodies |
front 290 What pathologic findings would be seen in a liver biopsy specimen
obtained from a patient with a history of alcoholism, jaundice,
hypoalbuminemia, and an elevated INR? | back 290 Sclerosis around central vein |
front 291 What does alcohol cessation lead to in patients with hepatic
steatosis? | back 291 reversal |
front 292 What pathologic features are seen in a liver biopsy specimen obtained
from a patient with hepatic steatosis? | back 292 Macrovesicular fatty change |
front 293 What is the likely diagnosis for a patient whose liver biopsy specimen shows regenerative nodules surrounded by fibrous bands? ____ ____ | back 293 Alcoholic cirrhosis |
front 294 What is the likely diagnosis for a patient with elevated liver enzymes and the findings on liver biopsy shown in the image? | back 294 hepatic steatosis |
front 295 What is the definition of gambling disorder? | back 295 manic |
front 296 What is the treatment of gambling disorder? | back 296 psychotherapy |
front 297 At what age does gender identity develop? | back 297 3 |
front 298 Is gender nonconformity a mental disorder? | back 298 No |
front 299 What is the definition of transgender? | back 299 different birth |
front 300 What is definition of gender dysphoria? | back 300 experiences birth |
front 301 Where is a drug made of large charged molecules or plasma protein-bound molecules typically distributed? _______ _______ | back 301 Intravascular compartment |
front 302 Where is a small hydrophilic drug with a medium volume of distribution typically distributed? _______ _______ | back 302 Extracellular fluid |
front 303 After 3 half-lives, what percentage of a drug remains if it was given
as a single-dose IV bolus? | back 303 12.5 |
front 304 Why is the bioavailability of a drug taken orally less than 100%? | back 304 Incomplete absorption of the drug |
front 305 bioavailability of IV drugs is _______ %. | back 305 100 |
front 306 After 1 half-life, given constant IV infusion of a drug, how close to
steady state is the concentration of the drug? | back 306 50 |
front 307 You administer a drug with a volume of distribution of 30 L and a clearance rate of 1.05 L/min. What is the half-life of this drug? | back 307 20 minutes t1/2 = ( 0.7 × Vd ) / CL |
front 308 In first-order kinetics, a drug infused at a constant rate takes ___ to ___ half-lives to reach steady state. | back 308 4, 5 |
front 309 What is the definition of the half-life of a drug? | back 309 half |
front 310 Disease in which three organs could impair drug clearance? | back 310 Heart Kidney Liver |
front 311 The half-life of a drug that follows first-order kinetics is 4 hours. How long after discontinuation of the drug until 6.25% of the drug remains? | back 311 16 hours |
front 312 What does clearance of a drug measure and how is it calculated? | back 312 Volume of plasma cleared of drug per unit time |
front 313 What is the embryologic origin of Schwann cells? ___ ___ | back 313 Neural crest |
front 314 What are the two main functions of Schwann cells? | back 314 Myelination regeneration |
front 315 Schwann cell injury, what disease? | back 315 Guillain-Barré syndrome |
front 316 How many axons does each Schwann cell myelinate? | back 316 1 |
front 317 What is the cell marker for Schwann cells? ___ | back 317 s100b |
front 318 What is indicated by the red arrow in the electron micrograph showing an axon in cross-section? | back 318 Myelin |
front 319 What cell types produce myelin in the central nervous system and the
peripheral nervous system? | back 319 Oligodendrocytes Schwann cells |
front 320 What does myelin do to an axon's space constant, conduction velocity,
membrane resistance, and membrane capacitance? | back 320 Increases space constant |
front 321 What role does myelin play in neuronal activity? | back 321 insulating increase |
front 322 How does myelin increase conduction velocity down an axon? | back 322 It promotes saltatory conduction at the nodes of Ranvier where concentrations of Na+ channels are high |
front 323 Which cranial nerves are myelinated as part of the central nervous
system and peripheral nervous system? | back 323 Central nervous system → Cranial nerve II |
front 324 What is the name of the phenomenon observed when a population undergoes a sharp reduction in population size, resulting in new allele frequencies? ____ ____ | back 324 Bottleneck effect |
front 325 What is the name of the phenomenon by which a dramatic change in allele frequency occurs by change, and not through natural selection? ____ ____ | back 325 Genetic drift |
front 326 What are the two major indications for intervention in a patient with a varicocele? ____ ____ | back 326 Pain |
front 327 What is the significance of a patient with a right-sided varicocele
that does not resolve when the patient lies supine? | back 327 inferior vena cava |
front 328 What are two major treatment options for patients with a varicocele? | back 328 ligation Embolization |
front 329 What is the major reason varicoceles are more common on the left side
of the body? | back 329 The left gonadal vein drains into the left renal vein → Increased venous pressure |
front 330 What is the pathophysiologic mechanism by which the pathology leads to infertility? _____ increase in the scrotum impairs spermatogenesis | back 330 temperature |
front 331 What is the pathophysiologic mechanism associated with the
development of a varicocele? | back 331 Increased venous pressure → Dilation of the pampiniform plexus |
front 332 What are two major ways to clinically diagnose a varicocele? | back 332 Ultrasound |
front 333 What is the definitive treatment for acromegaly? | back 333 Surgical resection of the pituitary adenoma |
front 334 What are three pharmacologic treatment options for acromegaly? | back 334 Pegvisomant |
front 335 What are three ways to diagnose acromegaly? | back 335 Lack of suppression of serum GH after oral glucose tolerance
tests |
front 336 What is the clinical implication of excess GH in children? | back 336 gigantism linear |
front 337 What is the most common cause of death in gigantism and acromegaly? | back 337 Heart failure |
front 338 What endocrine disease typically presents with an enlarged tongue with deep furrows, coarsening of facial features with age, deep voice, and frontal bossing? | back 338 Acromegaly |
front 339 How is glucose regulation affected in acromegaly? | back 339 resistance |
front 340 The patient shown in the image has noted difficulty speaking due to tongue enlargement. Based on this symptom and the physical exam findings shown, what is the diagnosis? | back 340 acromegaly |
front 341 What transports ADH and oxytocin from the hypothalamus to the posterior pituitary, where these hormones are stored and released? | back 341 Neurophysins |
front 342 Where in the hypothalamus are the hormones ADH and oxytocin produced? | back 342 supraoptic paraventricular |
front 343 Which region of the hypothalamus regulates parasympathetic activity
and induces you to cool off? | back 343 Anterior nucleus |
front 344 Which part of the hypothalamus regulates sleep and the circadian rhythm? | back 344 Suprachiasmatic nucleus |
front 345 How might a hypothalamic mass compressing the ventromedial nucleus present in a young patient? | back 345 Hyperphagia |
front 346 Which part of the hypothalamus regulates sympathetic activity and makes you to feel warm? [...] nucleus | back 346 Posterior nucleus |
front 347 What hormone regulates the ventromedial nucleus's function? _____ stimulates it | back 347 Leptin |
front 348 What area of the hypothalamus induces the sensation of satiety? _____ nucleus | back 348 Ventromedial nucleus |
front 349 An infant is born with hypoplastic lateral hypothalamic nuclei. How
does this condition manifest? | back 349 Failure to thrive |
front 350 What 2 hormones regulate the lateral nucleus of the hypothalamus? | back 350 Ghrelin stimulates |