Definition
Cohen syndrome is a very rare genetic disorder characterized by infantile hypotonia (a weakening of the skeletal muscles), childhood obesity, and several malformations.
Description
Cohen syndrome was first described in 1973 by Dr. M. M. Cohen, Jr. in three children with distinct physical and developmental observations. Since then, over 100 cases have been reported throughout the world, offering the picture of an extremely rare disease with a...
Source: Encyclopedia of Genetic Disorders, ©2002 Gale Cengage. All Rights Reserved. Full copyright.
(The entire page is 1937 words.)
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