A 6-year-old child is brought to the OPD with a history of mental retardation, failure to walk , failure to grow, seizures, hyperactivity, and tremors. On examination, there is microcephaly, fair hair, light skin color, and blue eyes. Which of the following enzyme is deficient in this child?

Correct Answer: Phenylalanine hydroxylase
Description: The given clinical manifestations point to the diagnosis of Phenylketonuria (PKU). Deficiency of the enzyme phenylalanine hydroxylase Reference: Harpers illustrated biochemistry 30th edition
Category: Anatomy
Share:

Get More
Subject Mock Tests

Practice with over 200,000 questions from various medical subjects and improve your knowledge.

Attempt a mock test now
Mock Exam

Take an exam with 100 random questions selected from all subjects to test your knowledge.

Coming Soon
Get More
Subject Mock Tests

Try practicing mock tests with over 200,000 questions from various medical subjects.

Attempt a mock test now
Mock Exam

Attempt an exam of 100 questions randomly chosen from all subjects.

Coming Soon
WordPress › Error

There has been a critical error on this website.

Learn more about troubleshooting WordPress.