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USMLE step 1 – biochemistry Practice Questions and Answers (100% Pass)

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USMLE step 1 – biochemistry Practice Questions and Answers (100% Pass) infant with somnolence, vomiting, cerebral edema, decreased BUN, hyperammonemia - Answer️️ -ornithine transcarbamoylase deficiency infantile cataracts, doesn't track objects, absent social smile - Answer️️ -galac...

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  • August 28, 2024
  • 16
  • 2024/2025
  • Exam (elaborations)
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  • USMLE
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©SOPHIABENNET@2024/2025 Tuesday, August 20, 202410:21 AM


USMLE step 1 – biochemistry Practice
Questions and Answers (100% Pass)

infant with somnolence, vomiting, cerebral edema, decreased BUN,
hyperammonemia - Answer✔️✔️-ornithine transcarbamoylase
deficiency

infantile cataracts, doesn't track objects, absent social smile -
Answer✔️✔️-galactokinase deficiency

infantile cataracts, hepatomegaly, jaundice, failure to thrive -
Answer✔️✔️-uridyltransferase deficiency

causes of Down syndrome - Answer✔️✔️-1) meiotic nondisjunction
(95%)

2) unbalanced robertsonian translocation (extra arm on Ch 21)

3) mosaic trisomy 21

treatment of hyperammonemia (HCV, urea cycle deficiency) -
Answer✔️✔️-limit protein in diet

benzoate, phenylbutarate (bind a.a.'s, increased aa exretion)

actulose (acidify GI tract, trap NH4 for excretion)

effect of hyperammonemia on metabolism - Answer✔️✔️-decreased
alpha ketoglutarate, inhibiting TCA cycle




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, ©SOPHIABENNET@2024/2025 Tuesday, August 20, 202410:21 AM


Tay-Sach's (enzyme, accumulated substance) - Answer✔️✔️-
hexosaminidase, GM2 ganglioside

metachromatic leukodystrophy (enzyme, accumulated substance) -
Answer✔️✔️-arylsulfatase, cerebroside sulfate

fabry's (enzyme, accumulated substance) - Answer✔️✔️-alpha-
galactosidase, ceramide trihexoside

krabbe's (enzyme, accumulated substance) - Answer✔️✔️-beta-
galactocerebrosidase, galactocerebroside

gauche's (enzyme, accumulated substance) - Answer✔️✔️-
glucocerebrosidase, glucocerebroside

niemann-pick - Answer✔️✔️-sphingomyelinase, sphingomyelin

hepatosplenomegaly, aseptic necrosis of femur, bone crises,
macrophages that look like crumpled tissue paper - Answer✔️✔️-
Gaucher's sphingolipidosis (glucocerebroside accumulation)

cherry macula, neurodegeneration, foam cells, hepatomegaly -
Answer✔️✔️-niemann-pick (sphyngomyelin)

cherry macula, neurodegenration, lysosomes with onion skin, NO
hepatisplenomegaly - Answer✔️✔️-tay-sachs (GM2 ganglioside)

causes of albinism - Answer✔️✔️-tyrosine transporter defect

tyrosine hydroxylase deficiency

lack of migration of neural crest cells (melanocytes)



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, ©SOPHIABENNET@2024/2025 Tuesday, August 20, 202410:21 AM


where do preganglionic parasympathetic neurons originate? -
Answer✔️✔️-nuclei of cranial nerves

sacral spinal cord (S2-S4)

where do preganglionic sympathetic neurons originate? -
Answer✔️✔️-thoracolumbar spinal cord (T1-L3)

arginine derivatives - Answer✔️✔️-creatine

urea (urea cycle intermediate)

NO

glutamate derivatives - Answer✔️✔️-GABA

glutathione

snRNPs - Answer✔️✔️-combine with pre-mRNA in nucleus to form
spliceosome to remove introns

what must happen in the nucleus so that 7-methylguanosine can
be added to RNA in the cytosol? - Answer✔️✔️-5' capping

what is the purpose of the mRNA 3' poly-A tail? - Answer✔️✔️-export
of mRNA from the nucleus

protection from enzymatic degradation in the cytoplasm

infant with coarse facial features, clouded corneas, restricted joint
movement - Answer✔️✔️-I cell disease: failure of mannose
phosphorylation of lysosome proteins in cis golgi --> lysosomal
enzymes are secreted outside the cell instead of sent to lysosome



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