Zoology - Principles of Inheritance and Variation Question with Solution | TestHub
ZoologyPrinciples of Inheritance and VariationGenetic DisordersEasy2 minPYQ_2020
ZoologyEasysingle choice
In phenylketonuria, the patient has a deficiency of any enzyme which
Options:
Answer:
A
Solution:
Phenylketonuria is an autosomal recessive disorder. In this disease, the patient cannot produce enzyme phenylalanine hydroxylase, which helps in conversion of phenylalanine to tyrosine. Thus, there is accumulation of phenylalanine and its derivatives in the body. Accumulation of these in brain results in mental retardation. These are also excreted through urine because of its poor absorption by kidney. The gene coding for phenylalanine hydroxylase is located on chromosome number 12.
Stream:NTA_ABHYAS_NEETSubject:ZoologyTopic:Principles of Inheritance and VariationSubtopic:Genetic Disorders
⏱ 2mℹ️ Source: PYQ_2020
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