Chapter·BiochemistryAmino acid metabolism and disorders

Branched-chain amino acid metabolismDownloads

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1

A 3-day-old female infant presents with poor feeding, lethargy, vomiting after feeding, and seizures. Labs revealed ketoacidosis and elevated hydroxypropionic acid levels. Upon administration of parenteral glucose and protein devoid of valine, isoleucine, methionine, and threonine, and carnitine, the infant began to recover. Which of the following enzymes is most likely deficient in this infant?

ABranched-chain ketoacid dehydrogenase

BPropionyl-CoA carboxylase

CCystathionine synthase

DPhenylalanine hydroxylase

EHomogentisate oxidase

2

A 29-year-old female presents to the family physician concerned over the blue-black discoloration of her sclera and skin. She notes that at the end of her day, there are black stains in her underwear. The incomplete breakdown of which of the following amino acids is responsible for this presentation?

ALeucine

BValine

CTyrosine

DMethionine

EIsoleucine

3

You are counseling a mother whose newborn has just screened positive for a deficit of phenylalanine hydroxylase enzyme. You inform her that her child will require dietary supplementation of which of the following?

AAspartame

BNiacin

CHomogentisic Acid

DTyrosine

ELeucine

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