Hereditary Motor and Sensory Neuropathies 03

Topic: Behavior

Created on Thursday, April 12 2007 by jdmiles

Last modified on Wednesday, August 17 2011.

 
        A) CMT-1A is associated with chromosomal location 1p35-36.
 
        B) Electrodiagnostic studies on patients with CMT-1A shows slowing of nerve conduction velocities.
 
        C) CMT-1A is associated with A-Galactosidase A.
 
        D) CMT-1A has an autosomal recessive inheritance pattern
 
        E) CMT-1A is associated with chromosomal location 4q12.
 

 

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This question was created on April 12, 2007 by jdmiles.
This question was last modified on August 17, 2011.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

ANSWERS AND EXPLANATIONS

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A) CMT-1A is associated with chromosomal location 1p35-36.

This answer is incorrect.

CMT-1A is associated with chromosomal location 17p11.2-12. Charcot-Marie-Tooth (CMT-2A) is associated with chromosomal location 1p35-36.   (See References)

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B) Electrodiagnostic studies on patients with CMT-1A shows slowing of nerve conduction velocities.

This answer is correct.

Electrodiagnostic studies on patients with CMT-1A shows slowing of nerve conduction velocities.  (See References)

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C) CMT-1A is associated with A-Galactosidase A.

This answer is incorrect.

CMT-1A is associated with peripheral myelin protein 22 (PMP-22). Sphingomyelinase is an enzyme which is deficient in Niemann-Pick disease type A.  (See References)

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D) CMT-1A has an autosomal recessive inheritance pattern

This answer is incorrect.

CMT-1A is a hereditary disease. In the majority of cases, the inheritance pattern of CMT-1A is autosomal dominant.  (See References)

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E) CMT-1A is associated with chromosomal location 4q12.

This answer is incorrect.

CMT-1A is associated with chromosomal location 17p11.2-12. Muscular dystrophy is associated with chromosomal location 4q12.   (See References)

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References:

1. Bashar Katirji... [et al.]. . Boston : Butterworth-Heinemann, c2002. (ISBN:0750671696)	Advertising:
2. Saporta, A.S., Sottile, S.L., Miller, L.J., Feely, S.M., Siskind, C.E., and Shy, M.E. (2011). "Charcot-Marie-Tooth disease subtypes and genetic testing strategies." Ann Neurol, 69(1) 22-33. (PMID:21280073)

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behavior
Hereditary Motor and Sensory Neuropathies 03
Question ID: 081711137
Question written by J. Douglas Miles, (C) 2006-2009, all rights reserved.
Created: 04/12/2007
Modified: 08/17/2011
Estimated Permutations: 60480