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Question

Biology Question on Mendelian Disorders

Study the pedigree chart given below. What does it show?

A

inheritance of a condition like phenylketonuria as an autosomal recessive trait

B

the pedigree chart is wrong as this is not possible

C

inheritance of a recessive sex-linked disease like haemophilia

D

inheritance of a sex-linked inborn error of metabolism like phenylketonuria

Answer

inheritance of a condition like phenylketonuria as an autosomal recessive trait

Explanation

Solution

This chart shows inheritance of an autosomal recessive trait like phenylketonuria. An autosomal recessive trait may skip a generation. It appears in case of marriage between two heterozygous individuals (Aa x Aa = 3 Aa + 1 aa), a recessive individual with hybrid (Aa x aa = 2 Aa + 2 aa) and two recessive (aa x aa = all aa). Phenylketonuria is an inborn, autosomal, recessive metabolic disorder in which homozygous recessive individual lacks the enzyme phenylalanine hydroxylase. The heterozygous individuals are normal but carriers.