U01.18.024 Phenylketonuria
17 Total attempts
amino acid metabolism, autosomal recessive, clinical biochemistry, dietary restriction, Genetic disorders, hypopigmentation, Inborn Errors of Metabolism, intellectual disability, Medical Flashcards, metabolic disorder, musty body odor, newborn screening, phenylalanine hydroxylase deficiency, phenylalanine metabolism, phenylketonuria, PKU, seizures, tyrosine metabolism, USMLE Step 1