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Biochemistry Phenylalanine and Tyrosine metabolism Detail 65051e0f

In Phenylketonuria, the first line therapy is:

A
Replacement of the defective enzyme
B
Replacement of the deficient product
C
Limiting the substrate for deficient enzyme
D
Giving the missing amino acid by diet
High-Yield Explanation
In phenylketonuria:- There is accumulation of phenylalanine Accumulated phenylalanine inhibits the transpo of other amino acids required for neurotransmitter synthesis, reduces synthesis and increases degradation of myelin - Mental retardation Breastfeeding introduces phenylalanine and symptoms will be:- 1. Vomiting 2. Irritability 3. Convulsions & tremors are the usual presentations. Thus, limiting the substrate of the deficient enzyme, i.e. phenylalanine, is the first-line of management. Breastfeeding should be avoided.

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