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Familial syndromic duodenal atresia: Feingold syndrome
M Holder-Espinasse1, Z Ahmad, J Hamill
1Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK.
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.
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