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NEUROLOGY MCQ – Exercise 51

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. most common subtype of CMT1 is

 
 
 
 

Q 2. autosomal recessive neuropathy includes

 
 
 
 

Q 3. Dejerine-sottas disease is also called as

 
 
 
 

Q 4. CMT1A subtype is caused by

 
 
 
 

Q 5. mutation in myelin protein zero gene mutation can produce

 
 
 
 

Q 6. CMT1 transmitted as

 
 
 
 

Q 7. role of P0

 
 
 
 

Q 8. protein restricted to CNS myelin

 
 
 
 

Q 9. in CMT1 motor conduction velocities in the arms slowed to

 
 
 
 

Q 10. CMT disease includes

 
 
 
 

Q 11. Charcot-Marie –Tooth disease includes

 
 
 
 

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

 
 
 
 

Q 13. myelin includes all except

 
 
 
 

Q 14. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 15. Schmidt Lanterman incisures include

 
 
 
 

Q 16. ratio of occurrence of CMT1:CMT2 is approximately

 
 
 
 

Q 17. most common type of hereditary neuropathy

 
 
 
 

Q 18. which manifestation indicates CMT1

 
 
 
 

Q 19. Dejerine-sottas syndrome is caused by point mutations of

 
 
 
 

Q 20. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 21. various subtypes of CMT are classified according to

 
 
 
 

Q 22. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 23. infantile onset or severe childhood forms of CMT include

 
 
 
 

Q 24. role of PMP22 includes

 
 
 
 

Q 25. CMT2 is caused by mutations in which gene

 
 
 
 

Q 26. tomaculous neuropathy includes

 
 
 
 

Q 27. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 28. CMT transmitted as

 
 
 
 

Q 29. gap junction membrane spanning proteins expressed by schwann cells are called

 
 
 
 

Q 30. which manifestation indicates CMT1

 
 
 
 


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