PHARMACOLOGY NBME EXAM (ACTUAL
EXAM) WITH CORRECT ACTUAL
QUESTIONS AND CORRECTLY WELL
DEFINED ANSWERS LATEST ALREADY
GRADED A+ 2026
McArdle's disease - ANSWERS-Type V glycogen storage
disease
Defect in glycogen phosphorylase (muslce)
Excercised incuded cramps
Pompe's Disease - ANSWERS-Type II glycogen storage
disease (stuck in lysosome)
Mutation in acid alpha-glycosidase
Failure to thrive
Von Gerke's disease - ANSWERS-Type I glycogen storage
disease
Increased liver glycogen, severe fastting hypoglycemia
,Defect in glucose 6-phosphatase
Aceyl-CoA dehydrogenase deficiency - ANSWERS-
hypoglycemia in fasting
cardiomyopathy
Lipopritein lipase deficiency - ANSWERS-
hyperchylomicronemia, dyslipidemia
Derivatives of Phenylalanine - ANSWERS-melanin,
Dopamine, norepinephrine, epinephrine
Tryptophan derivatives - ANSWERS-niacin, serotonin,
melatonin
Glycine derivative - ANSWERS-porphyrin
Arginine deriviatives - ANSWERS-creatine, NO
Glutamate derivatives - ANSWERS-GABA, glutathione
, PKU enzyme and symptoms - ANSWERS-mutation in
phenylalanine hydroxylase
accumulation of pphenalalnine deriviatives
Alkaptonuria - ANSWERS-problems with homogenistic acid
oxidase
Dark connective tissue, black urine
Albinism - ANSWERS-defeciency in tyrosinase or tyrosine
transporters
Homocystinuria - ANSWERS-deficiency of cystathione
synthase or homocystine methyltransferase
can produce methionine incrase, tall stature chest
deformities, homocystine in urine
Cystinuria - ANSWERS-problems with renal tubular amino
acid transporters
crystals in urine
Maple syrup Urine disease - ANSWERS-branched chain
alpha-keto acid denydrogenas
EXAM) WITH CORRECT ACTUAL
QUESTIONS AND CORRECTLY WELL
DEFINED ANSWERS LATEST ALREADY
GRADED A+ 2026
McArdle's disease - ANSWERS-Type V glycogen storage
disease
Defect in glycogen phosphorylase (muslce)
Excercised incuded cramps
Pompe's Disease - ANSWERS-Type II glycogen storage
disease (stuck in lysosome)
Mutation in acid alpha-glycosidase
Failure to thrive
Von Gerke's disease - ANSWERS-Type I glycogen storage
disease
Increased liver glycogen, severe fastting hypoglycemia
,Defect in glucose 6-phosphatase
Aceyl-CoA dehydrogenase deficiency - ANSWERS-
hypoglycemia in fasting
cardiomyopathy
Lipopritein lipase deficiency - ANSWERS-
hyperchylomicronemia, dyslipidemia
Derivatives of Phenylalanine - ANSWERS-melanin,
Dopamine, norepinephrine, epinephrine
Tryptophan derivatives - ANSWERS-niacin, serotonin,
melatonin
Glycine derivative - ANSWERS-porphyrin
Arginine deriviatives - ANSWERS-creatine, NO
Glutamate derivatives - ANSWERS-GABA, glutathione
, PKU enzyme and symptoms - ANSWERS-mutation in
phenylalanine hydroxylase
accumulation of pphenalalnine deriviatives
Alkaptonuria - ANSWERS-problems with homogenistic acid
oxidase
Dark connective tissue, black urine
Albinism - ANSWERS-defeciency in tyrosinase or tyrosine
transporters
Homocystinuria - ANSWERS-deficiency of cystathione
synthase or homocystine methyltransferase
can produce methionine incrase, tall stature chest
deformities, homocystine in urine
Cystinuria - ANSWERS-problems with renal tubular amino
acid transporters
crystals in urine
Maple syrup Urine disease - ANSWERS-branched chain
alpha-keto acid denydrogenas
