Article
Familial syndromic esophageal atresia maps to 2p23-p24.
American journal of human genetics - 1 Feb 2000
Celli J, van Beusekom E, Hennekam R C, Gallardo M E, Smeets D F, de Córdoba S R, Innis J W, Frydman M, König R, Kingston H, Tolmie J, Govaerts L C, van Bokhoven H, Brunner H G
Abstract excerpt
Esophageal atresia (EA) is a common life-threatening congenital anomaly that occurs in 1/3,000 newborns. Little is known of the genetic factors that underlie EA. Oculodigitoesophageoduodenal (ODED) syndrome (also known as "Feingold syndrome") is a rare autosomal dominant disorder with digital abnormalities, microcephaly, short palpebral fissures, mild learning disability, and esophageal/duodenal atresia. We...
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