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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. various subtypes of CMT are classified according to

 
 
 
 

Q 2. Dejerine-sottas disease is also called as

 
 
 
 

Q 3. which manifestation indicates CMT1

 
 
 
 

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

 
 
 
 

Q 5. CMT1A subtype is caused by

 
 
 
 

Q 6. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 7. gap junction membrane spanning proteins expressed by schwann cells are called

 
 
 
 

Q 8. most common subtype of CMT1 is

 
 
 
 

Q 9. Charcot-Marie –Tooth disease includes

 
 
 
 

Q 10. CMT1 transmitted as

 
 
 
 

Q 11. protein restricted to CNS myelin

 
 
 
 

Q 12. CMT transmitted as

 
 
 
 

Q 13. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 14. Pelizeaus Merzbacher disease is caused by mutations in gene for

 
 
 
 

Q 15. most common type of hereditary neuropathy

 
 
 
 

Q 16. mutation in myelin protein zero gene mutation can produce

 
 
 
 

Q 17. ratio of occurrence of CMT1:CMT2 is approximately

 
 
 
 

Q 18. CMT disease includes

 
 
 
 

Q 19. role of P0

 
 
 
 

Q 20. Schmidt Lanterman incisures include

 
 
 
 

Q 21. tomaculous neuropathy includes

 
 
 
 

Q 22. myelin includes all except

 
 
 
 

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

 
 
 
 

Q 24. CMT2 is caused by mutations in which gene

 
 
 
 

Q 25. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 26. Dejerine-sottas syndrome is caused by point mutations of

 
 
 
 

Q 27. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 28. autosomal recessive neuropathy includes

 
 
 
 

Q 29. which manifestation indicates CMT1

 
 
 
 

Q 30. role of PMP22 includes

 
 
 
 


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