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NEUROLOGY MCQ – Exercise 51

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. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 2. which manifestation indicates CMT1

 
 
 
 

Q 3. mutation in myelin protein zero gene mutation can produce

 
 
 
 

Q 4. CMT disease includes

 
 
 
 

Q 5. Dejerine-sottas disease is also called as

 
 
 
 

Q 6. role of P0

 
 
 
 

Q 7. Charcot-Marie –Tooth disease includes

 
 
 
 

Q 8. which manifestation indicates CMT1

 
 
 
 

Q 9. most common subtype of CMT1 is

 
 
 
 

Q 10. ratio of occurrence of CMT1:CMT2 is approximately

 
 
 
 

Q 11. Pelizeaus Merzbacher disease is caused by mutations in gene for

 
 
 
 

Q 12. CMT2 is caused by mutations in which gene

 
 
 
 

Q 13. autosomal recessive neuropathy includes

 
 
 
 

Q 14. CMT1A subtype is caused by

 
 
 
 

Q 15. Dejerine-sottas syndrome is caused by point mutations of

 
 
 
 

Q 16. most common type of hereditary neuropathy

 
 
 
 

Q 17. myelin includes all except

 
 
 
 

Q 18. in CMT1 motor conduction velocities in the arms slowed to

 
 
 
 

Q 19. various subtypes of CMT are classified according to

 
 
 
 

Q 20. Schmidt Lanterman incisures include

 
 
 
 

Q 21. gap junction membrane spanning proteins expressed by schwann cells are called

 
 
 
 

Q 22. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 23. CMT1 transmitted as

 
 
 
 

Q 24. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 25. tomaculous neuropathy includes

 
 
 
 

Q 26. protein restricted to CNS myelin

 
 
 
 

Q 27. infantile onset or severe childhood forms of CMT include

 
 
 
 

Q 28. CMT transmitted as

 
 
 
 

Q 29. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 30. role of PMP22 includes

 
 
 
 


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