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Title: Familial syndromic duodenal atresia: Feingold syndrome. Author: Holder-Espinasse M, Ahmad Z, Hamill J, Pahari A, Misra D, Drake D, Winter RM, Wilson LC. Journal: Eur J Pediatr Surg; 2004 Apr; 14(2):112-6. PubMed ID: 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.[Abstract] [Full Text] [Related] [New Search]