| Literature DB >> 671157 |
Abstract
In 1973 Cohen et al reported a new syndrome in two siblings and an unrelated individual, consisting of obesity, mental retardation, hypotonia, limb abnormalities, and a characteristic craniofacial appearance. Since then no similar cases have appeared in the literature. This report firmly establishes the Cohen syndrome as a distinct clinical entity by presenting four additional patients, including a sibling pair of normal parents, suggesting autosomal recessive inheritance. One of our four patients has normal intelligence, indicating that mental deficiency is a variable feature of the syndrome.Entities:
Mesh:
Year: 1978 PMID: 671157 DOI: 10.1016/s0022-3476(78)80504-6
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406