In phenylketonuria:

  • A
    Breakdown of phenylalanine is rapid
  • B
    Accumulation of phenylalanine in body
  • C
    Chromosomal constitution of patient changes
  • D
    $TSD$ gene situated on chromosome $15$ undergoes mutation

Explore More

Similar Questions

Hemophilia is more common in human males than in females because it is a:

$A$ normal-visioned woman, whose father is colour-blind, marries a normal-visioned man. What would be the probability of her sons and daughters being colour-blind? Explain with the help of a pedigree chart.

Which of the following diseases is known as a 'bleeder's disease',caused by the presence of an $X$-linked recessive gene?

$A$ son of a colourblind father and a normal homozygous mother marries a daughter of a normal father and a heterozygous (carrier) mother. What will be the phenotype of their children?

The 'Thala test' is performed for the confirmation of:

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo