Your browser doesn't support javascript.
loading
Familial syndromic duodenal atresia: Feingold syndrome.
Holder-Espinasse, M; Ahmad, Z; Hamill, J; Pahari, A; Misra, D; Drake, D; Winter, R M; Wilson, L C.
Affiliation
  • Holder-Espinasse M; Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK.
Eur J Pediatr Surg ; 14(2): 112-6, 2004 Apr.
Article in En | MEDLINE | ID: mdl-15185158
ABSTRACT
Familial duodenal atresia occurs as part of Feingold syndrome. Other features of this variable autosomal dominant condition include tracheo-oesophageal fistula and oesophageal atresia, microcephaly, hand and foot anomalies, facial dysmorphism, and developmental delay. We report a father and two sons with Feingold syndrome. One has bilateral dysplastic kidneys which have not been reported previously.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Duodenal Obstruction / Intestinal Atresia Limits: Humans / Male Language: En Journal: Eur J Pediatr Surg Journal subject: PEDIATRIA Year: 2004 Document type: Article Affiliation country: United kingdom
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Duodenal Obstruction / Intestinal Atresia Limits: Humans / Male Language: En Journal: Eur J Pediatr Surg Journal subject: PEDIATRIA Year: 2004 Document type: Article Affiliation country: United kingdom