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Given the current detection rate, failure to identify a disease-causing sequence variant does not preclude the diagnosis of Alström syndrome.
 
 
Sensitivity and specificity of the above test are 96% and 100% respectively.  Given the current detection rate, failure to identify a disease-causing sequence variant does not preclude the diagnosis of Alström syndrome.


==References==
==References==

Revision as of 15:46, 22 February 2013

Alstrom syndrome Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1], Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2]; Raviteja Guddeti, M.B.B.S. [3]

Other Diagnostic Studies

Molecular Genetic Testing

Gene Testing Method Detected Mutations
ALMS1 Targeted mutation analysis 19-bp insertion exon 16
ALMS1 Sequence analysis of select exons: 16, 10, and 8 Sequence variants
ALMS1 Sequence analysis of entire coding region Sequence variants
ALMS1 Deletion / duplication analysis Exonic and whole-gene deletions


Sensitivity and specificity of the above test are 96% and 100% respectively. Given the current detection rate, failure to identify a disease-causing sequence variant does not preclude the diagnosis of Alström syndrome.

References


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