Answer -- A. Phenylketonuria
Deficiency of phenylalanine hydroxylase
1:10,000
Autosomal recessive
mental retardation, hyperactivity, seizures, light complexion, eczema
Newborn screening
Back to question
Back to Practice Question and Answer--- Foundation of Practice
Deficiency of phenylalanine hydroxylase
1:10,000
Autosomal recessive
mental retardation, hyperactivity, seizures, light complexion, eczema
Newborn screening
Back to question
Back to Practice Question and Answer--- Foundation of Practice
NAVIGATION
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QUESTION BANK-- AKP
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