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NEUROLOGY MCQ – Exercise 32

By | Published: October 12, 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. retinal pigmentary degeneration occurs in which type of SCAs

 
 
 
 

Q 2. Amyotrophic lateral sclerosis-Parkinsonism-dystonia type presentation is in which clinical type of MJD

 
 
 
 

Q 3. gene related to DRPLA

 
 
 
 

Q 4. dynamic mutation refers to that in subsequent generations; expanded repeat may increase further in length and result in

 
 
 
 

Q 5. symmetric ataxia caused by all except

 
 
 
 

Q 6. most common form of inherited ataxia is

 
 
 
 

Q 7. which trinucleotide repeats disorders has autosomal recessive inheritance

 
 
 
 

Q 8. paraneoplastic opsoclonus-myoclonus syndrome is related to

 
 
 
 

Q 9. patient fall over backwards in

 
 
 
 

Q 10. in SCA7 color blindness is for which color

 
 
 
 

Q 11. symmetric ataxia is caused by

 
 
 
 

Q 12. Para neoplastic cerebellar ataxia associated with anti-PQ type voltage gated calcium channel autoantibody occurs in which tumor

 
 
 
 

Q 13. ataxic-amyotrophic type presentation is seen in which type of MJD

 
 
 
 

Q 14. most common inherited autosomal dominant spinocerebellar ataxia

 
 
 
 

Q 15. Haw River syndrome an autosomal dominant neurodegenerative disease associated with

 
 
 
 

Q 16. true cerebellar ataxia result from the involvement of

 
 
 
 

Q 17. which spinocetrebellar ataxia is caused by an untranslated pentanucleotide repeat

 
 
 
 

Q 18. patient retain full intellectual function in which clinical type of MJD

 
 
 
 

Q 19. ataxins are

 
 
 
 

Q 20. the mean age of onset of symptoms in MJD is

 
 
 
 

Q 21. expanded polyglutamine ataxins with more than how many glutaminesare potentially toxic to neurons

 
 
 
 

Q 22. which spinocerebellar ataxia is referred as olivopontocerebellar atrophy

 
 
 
 

Q 23. CAG repeat diseases includes

 
 
 
 

Q 24. Para neoplastic cerebellar ataxia is associated with

 
 
 
 

Q 25. which type of spinocerebellar ataxia is most common in India

 
 
 
 

Q 26. true statement regarding increase in number of nucleotide repeats is false

 
 
 
 

Q 27. in MJD which is spared

 
 
 
 

Q 28. most common clinical type of MJD

 
 
 
 

Q 29. ataxic type presentation is seen in which type of MJD

 
 
 
 

Q 30. which type of SCA has pure cerebellar presentation

 
 
 
 


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