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NEUROLOGY MCQ – Exercise 59

By | Published: October 13, 2015

The multiple choice questions in this online test paper focuses on NEUROLOGY MCQ. If you are looking for self evaluation of your PG Medical entrance exam preparation then this online NEUROLOGY MCQ Test Paper will help you to evaluate your exam preparation.

Instruction for REPRODUCTIVE BIOLOGY/ REPRODUCTIVE MEDICINE / INFERTILITY MCQs:

1- This online MCQ practice test paper contains 30 questions.
2- Each question in this online practice test paper have four options and only 1 option is correct.
3- You can view the answers of this practice test paper after submitting the practice test paper.
Note: The answers mentioned at the end of practice test are the best suitable option as per our knowledge. Users shall cross-check the answers with their textbooks.

Q 1. Hatchet faced appearance is seen in

 
 
 
 

Q 2. regarding calpain true is

 
 
 
 

Q 3. principal source of energy for skeletal muscles

 
 
 
 

Q 4. muscular dystrophy with onset at birth includes

 
 
 
 

Q 5. dystrophin binds to which of the following in sarcolemma

 
 
 
 

Q 6. patient of DMD are typically in wheelchair by the age of

 
 
 
 

Q 7. severe brain impairment is seen in which congenital muscular dystrophy

 
 
 
 

Q 8. gastrocnemius muscles are preferentially affected at onset in

 
 
 
 

Q 9. Gower’s maneuver is diagnostic of

 
 
 
 

Q 10. which congenital myopathies are susceptible to malignant hyperthermia

 
 
 
 

Q 11. patient with Becker`s muscular dystrophy first experience difficulties at what age

 
 
 
 

Q 12. alpha glucosidase or acid maltase deficiency is also called

 
 
 
 

Q 13. which distal myopathy begins in hands

 
 
 
 

Q 14. true regarding DMD is all except

 
 
 
 

Q 15. in DMD there is preferential involvement of which muscle group

 
 
 
 

Q 16. LGMD2A is caused by mutations in

 
 
 
 

Q 17. Becker`s muscular dystrophy resembles

 
 
 
 

Q 18. antimyotonia drug include

 
 
 
 

Q 19. variant of LGMD2B is

 
 
 
 

Q 20. key defect in DMD due to abnormal dystrophin protein is

 
 
 
 

Q 21. LGMD2B is due to defect in

 
 
 
 

Q 22. muscle relatively spared in Facioscapulohumeral muscular dystrophy

 
 
 
 

Q 23. congenital myopathy includes

 
 
 
 

Q 24. calpains are Ca2+ dependent

 
 
 
 

Q 25. which distal myopathy begins in lower limbs

 
 
 
 

Q 26. tissue specific calpains have been implicated in

 
 
 
 

Q 27. uncommon cause of death in DMD

 
 
 
 

Q 28. which significantly slows progression of DMD

 
 
 
 

Q 29. CK levels in DMD disease include

 
 
 
 

Q 30. Gower`s sign is due to weakness in muscles of

 
 
 
 


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