Copy of Sjogren-Larsson Syndrome 01

Topic: Pediatric

Created on Sunday, February 24 2008 by jdmiles

Last modified on Sunday, February 24 2008.

 
        A) It is associated with an acid ceramidase deficiency
 
        B) It is associated with a defect on chromosome 3
 
        C) It is associated with a defect on chromosome 17
 
        D) It has autosomal dominant inheritance
 
        E) Symtpoms include psychosis, angular stomatosis, and periodic peripheral neuropathy
 

 

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This question was created on February 24, 2008 by jdmiles.
This question was last modified on February 24, 2008.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

ANSWERS AND EXPLANATIONS

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A) It is associated with an acid ceramidase deficiency

This answer is incorrect.

Acid ceramidase is an enzyme which is deficient in Farber disease   (See References)

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B) It is associated with a defect on chromosome 3

This answer is incorrect.

Sjögren-Larsson syndrome is a rare, autosomal recessive disease associated with a defect on chromosome 17.   (See References)

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C) It is associated with a defect on chromosome 17

This answer is correct.

Sjögren-Larsson syndrome is a rare, autosomal recessive neurocutaneous disorder (phakomatosis). Patients present with ichthyosis, mental retardation, and spasticity. It is associated with a mutation in the gene encoding fatty aldehyde dehydrogenase, located on chromosome 17.   (See References)

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D) It has autosomal dominant inheritance

This answer is incorrect.

Sjögren-Larsson syndrome is a rare, autosomal recessive neurocutaneous disorder (phakomatosis). Patients present with ichthyosis, mental retardation, and spasticity. It is associated with a mutation in the gene encoding fatty aldehyde dehydrogenase, located on chromosome 17.   (See References)

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E) Symtpoms include psychosis, angular stomatosis, and periodic peripheral neuropathy

This answer is incorrect.

Sjögren-Larsson syndrome is a rare, autosomal recessive neurocutaneous disorder (phakomatosis). Patients present with ichthyosis, mental retardation, and spasticity. It is associated with a mutation in the gene encoding fatty aldehyde dehydrogenase, located on chromosome 17.   (See References)

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References:

1. Haug, S., and Braun-Falco, M. (2006). "Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome." Gene Ther, 13(13) 1021-6. (PMID:16525484)
2. Willemsen, M.A., Cruysberg, J.R., Rotteveel, J.J., Aandekerk, A.L., Van Domburg, P.H., and Deutman, A.F. (2000). "Juvenile macular dystrophy associated with deficient activity of fatty aldehyde dehydrogenase in Sjögren-Larsson syndrome." Am J Ophthalmol, 130(6) 782-9. (PMID:11124298)
3. Pastores, G.M. and Kolodny, E.H. (2004). Inborn errors of metabolism of the nervous system. In Bradley, W.G., Daroff, R.B., Fenichel, G.M., and Jankovic, J. (Eds.). Neurology in Clinical Practice, Fourth Edition. Butterworth Heinemann, Philadelphia, pp. 1811-1832 (ISBN:0750674695).	Advertising:
4. Ramelli, G.P., Slongo, T., Weis, J., Tschäppler, H., and Vassella, F. (). "[Pseudoarthrosis in neurofibromatosis type 1]" Klin Padiatr, 212(1) 26-30. (PMID:10719680)

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pediatric
Copy of Sjogren-Larsson Syndrome 01
Question ID: 022408158
Question written by J. Douglas Miles, (C) 2006-2009, all rights reserved.
Created: 02/24/2008
Modified: 02/24/2008
Estimated Permutations: 356400