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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. protein restricted to CNS myelin

 
 
 
 

Q 2. CMT transmitted as

 
 
 
 

Q 3. Dejerine-sottas syndrome is similar to

 
 
 
 

Q 4. which manifestation indicates CMT1

 
 
 
 

Q 5. ratio of occurrence of CMT1:CMT2 is approximately

 
 
 
 

Q 6. CMT2 is caused by mutations in which gene

 
 
 
 

Q 7. role of P0

 
 
 
 

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

 
 
 
 

Q 9. which manifestation indicates CMT1

 
 
 
 

Q 10. most common type of hereditary neuropathy

 
 
 
 

Q 11. CMT1 transmitted as

 
 
 
 

Q 12. tomaculous neuropathy includes

 
 
 
 

Q 13. Dejerine-sottas disease is also called as

 
 
 
 

Q 14. Charcot-Marie –Tooth disease includes

 
 
 
 

Q 15. palpable thickened nerves in CMT1 is due to increase in

 
 
 
 

Q 16. CMT1A subtype is caused by

 
 
 
 

Q 17. CMT disease includes

 
 
 
 

Q 18. Dejerine-sottas syndrome is caused by point mutations of

 
 
 
 

Q 19. Schmidt Lanterman incisures include

 
 
 
 

Q 20. autosomal recessive neuropathy includes

 
 
 
 

Q 21. role of PMP22 includes

 
 
 
 

Q 22. mutation in myelin protein zero gene mutation can produce

 
 
 
 

Q 23. Pelizeaus Merzbacher disease is caused by mutations in gene for

 
 
 
 

Q 24. infantile onset or severe childhood forms of CMT include

 
 
 
 

Q 25. myelin includes all except

 
 
 
 

Q 26. most common subtype of CMT1 is

 
 
 
 

Q 27. characteristic nerve biopsy appearance in CMT1 is

 
 
 
 

Q 28. CMT1B subtype is caused by mutations in gene for

 
 
 
 

Q 29. various subtypes of CMT are classified according to

 
 
 
 

Q 30. in CMT1 motor conduction velocities in the arms slowed to

 
 
 
 


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