Complete Information on Cohen syndrome
June 6th, 2008
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Cohen Syndrome is an uncommon hereditary disorder caused by a recessive gene. Cohen Syndromeis characterized by childish hypotonia (a weakening of the bony muscles), childhood obesity, and several malformations.
Cohen syndrome has several characteristics such as obesity, psychological retardation and craniofacial dysmorphism. It has an autosomal recessive infection with varying manifestation Cohen syndrome has too been referred to as Pepper syndrome, Hypotonia-Obesity-Prominent Incisors syndrome, Obesity-Hypotonia syndrome, and Mirhosseini-Holmes-Walton syndrome.
