Asked by Karina Rodriguez on Jun 18, 2024
Verified
Phenylketonuria is
A) an enzyme disorder.
B) transmitted by a dominant gene.
C) a disorder that manifests itself in all children of carriers.
D) an illness that can only occur in boys.
Phenylketonuria
A genetic disorder resulting in the inability to metabolize the amino acid phenylalanine, necessitating a strict diet to prevent intellectual disability.
Enzyme Disorder
A medical condition resulting from deficiencies or malfunctions of enzymes, affecting bodily processes.
- Acknowledge the relationship between genetic disorders and their impact on physical, cognitive, or developmental outcomes.
- Appreciate the value of immediate action and diet regulation in congenital metabolic disorders.
Verified Answer
VC
Vanessa CalvacheJun 23, 2024
Final Answer :
A
Explanation :
Phenylketonuria (PKU) is a metabolic disorder caused by a deficiency of the enzyme phenylalanine hydroxylase, which is necessary for the metabolism of the amino acid phenylalanine.
Learning Objectives
- Acknowledge the relationship between genetic disorders and their impact on physical, cognitive, or developmental outcomes.
- Appreciate the value of immediate action and diet regulation in congenital metabolic disorders.
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