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Imperforate anus in Feingold syndrome

✍ Scribed by B�ttiker, Vera; Wojtulewicz, Julian; Wilson, Meredith

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
18 KB
Volume
92
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(20000529)92:3<166::aid-ajmg2>3.0.co;2-#

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✦ Synopsis

A father and daughter had the characteristic findings of Feingold syndrome including microcephaly, short palpebral fissures, brachydactyly with clinodactyly of fifth fingers, and bilateral syndactyly of second to third and fourth to fifth toes. The infant presented with long-gap esophageal atresia without fistula (type A). Her father, who had short stature and learning disabilities, had congenital imperforate anus with a rectovesical fistula. This is the first report of distal intestinal atresia in Feingold syndrome.

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