𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Familial syndromic duodenal atresia: Feingold syndrome

Book ID
116684962
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
46 KB
Volume
40
Category
Article
ISSN
0022-3468

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Syndrome de Feingold
Syndrome de Feingold
✍ J.L. Alessandri; D. Graber; I. Tiran-Rajaofera; A. Montbrun; H. Pilorget; S. Sam πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 461 KB
Feingold syndrome: Report of a new famil
Feingold syndrome: Report of a new family and review
✍ Courtens, W.; Levi, S.; Verbelen, F.; Verloes, A.; Vamos, E. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 41 KB πŸ‘ 3 views

Feingold syndrome (or oculodigitoesophagoduodenal syndrome; Microcephaly, Mesobrachyphalangy, Tracheo-esophageal fistula syndrome) is a dominantly inherited combination of hand and foot abnormalities, microcephaly, esophageal/duodenal atresia, short palpebral fissures and learning disabilities, firs

Imperforate anus in Feingold syndrome
Imperforate anus in Feingold syndrome
✍ BοΏ½ttiker, Vera; Wojtulewicz, Julian; Wilson, Meredith πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 18 KB πŸ‘ 1 views

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 w