Digg StumbleUpon LinkedIn YouTube Flickr Facebook Twitter RSS Reset
Comments Off

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. tomaculous neuropathy includes

 
 
 
 

Q 2. mutation in myelin protein zero gene mutation can produce

 
 
 
 

Q 3. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 4. Dejerine-sottas syndrome is caused by point mutations of

 
 
 
 

Q 5. which manifestation indicates CMT1

 
 
 
 

Q 6. CMT1A subtype is caused by

 
 
 
 

Q 7. CMT1 transmitted as

 
 
 
 

Q 8. gap junction membrane spanning proteins expressed by schwann cells are called

 
 
 
 

Q 9. protein restricted to CNS myelin

 
 
 
 

Q 10. Charcot-Marie –Tooth disease includes

 
 
 
 

Q 11. CMT2 is caused by mutations in which gene

 
 
 
 

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

 
 
 
 

Q 13. CMT disease includes

 
 
 
 

Q 14. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 15. ratio of occurrence of CMT1:CMT2 is approximately

 
 
 
 

Q 16. most common type of hereditary neuropathy

 
 
 
 

Q 17. infantile onset or severe childhood forms of CMT include

 
 
 
 

Q 18. most common subtype of CMT1 is

 
 
 
 

Q 19. role of P0

 
 
 
 

Q 20. in CMT1 motor conduction velocities in the arms slowed to

 
 
 
 

Q 21. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 22. role of PMP22 includes

 
 
 
 

Q 23. which manifestation indicates CMT1

 
 
 
 

Q 24. Dejerine-sottas disease is also called as

 
 
 
 

Q 25. myelin includes all except

 
 
 
 

Q 26. autosomal recessive neuropathy includes

 
 
 
 

Q 27. various subtypes of CMT are classified according to

 
 
 
 

Q 28. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 29. Schmidt Lanterman incisures include

 
 
 
 

Q 30. CMT transmitted as

 
 
 
 


Comments are closed.