Cohen syndrome

Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity.

Arachnodactyly

Abnormally long and slender fingers (\"spider fingers\").


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PMID (PMCID)
24640185
(4345665)
 MIXED_SAMPLE
Surgical treatment for kyphoscoliosis in Cohen syndrome.
Imagama S, Tsuji T, Ohara T, Katayama Y, Goto M, Ishiguro N, Kawakami N.
Nagoya J Med Sci. 2013;75(3-4):279-86.
The patient was a 14-year-old male with the characteristics of Cohen syndrome: truncal obesity, mental retardation, arachnodactyly, microcephalia, and a facial malformation.