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Cohen Syndrome Community

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Community Members: 3

Brief Description

Cohen Syndrome is believed to be a gene mutation at locus 8q22 gene COH1 and is characterized by obesity, mental retardation and craniofacial dysmorphism.

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Synonyms

Pepper Syndrome, Cervenka Syndrome

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Community Members

1. 

   wendybiggins

   

   gsmom

   

   Lynn