Hypokalemic periodic paralysis is inherited as an autosomal dominant disorder with incomplete penetrance; it is resulted because of mutation in:

Correct Answer: Calcium channel
Description: Ans. D. Calcium channelHypokalemic Periodic Paralysis* Onset occurs at adolescence.* Men are more often affected because of decreased penetrance in women.* Hypokalemic periodic paralysis is inherited as an autosomal dominant disorder with incomplete penetrance.* Mutations in the voltage-sensitive, skeletal muscle calcium channel cause the disease.
Category: Medicine
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.