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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. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 2. most common type of hereditary neuropathy

 
 
 
 

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

 
 
 
 

Q 4. in CMT1 motor conduction velocities in the arms slowed to

 
 
 
 

Q 5. CMT1A subtype is caused by

 
 
 
 

Q 6. Dejerine-sottas disease is also called as

 
 
 
 

Q 7. CMT disease includes

 
 
 
 

Q 8. role of P0

 
 
 
 

Q 9. most common subtype of CMT1 is

 
 
 
 

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

 
 
 
 

Q 11. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 12. Pelizeaus Merzbacher disease is caused by mutations in gene for

 
 
 
 

Q 13. Charcot-Marie –Tooth disease includes

 
 
 
 

Q 14. gap junction membrane spanning proteins expressed by schwann cells are called

 
 
 
 

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

 
 
 
 

Q 16. which manifestation indicates CMT1

 
 
 
 

Q 17. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 18. infantile onset or severe childhood forms of CMT include

 
 
 
 

Q 19. CMT1 transmitted as

 
 
 
 

Q 20. protein restricted to CNS myelin

 
 
 
 

Q 21. Schmidt Lanterman incisures include

 
 
 
 

Q 22. myelin includes all except

 
 
 
 

Q 23. tomaculous neuropathy includes

 
 
 
 

Q 24. CMT2 is caused by mutations in which gene

 
 
 
 

Q 25. role of PMP22 includes

 
 
 
 

Q 26. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 27. various subtypes of CMT are classified according to

 
 
 
 

Q 28. which manifestation indicates CMT1

 
 
 
 

Q 29. autosomal recessive neuropathy includes

 
 
 
 

Q 30. CMT transmitted as

 
 
 
 


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