Duodenal atresia

Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen.

Short palpebral fissure

Distance between the medial and lateral canthi is more than 2 SD below the mean for age (objective); or, apparently reduced length of the palpebral fissures.


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PMID (PMCID)
19852433
 MALE Infant
A Feingold syndrome case with previously undescribed features and a new mutation.
Kocak H, Ozaydin E, Kose G, Marcelis CL, Kamsteeg EJ, Ceylaner S.
Genet Couns. 2009;20(3):261-7.
Feingold syndrome (FS) is a dominantly inherited combination of microcephaly with or without learning disabilities, hand and foot abnormalities, short palpebral fissures and esophageal/duodenal atresia.
10911531
 MALE Infant
[Feingold syndrome].
Alessandri JL, Graber D, Tiran-Rajaofera I, Montbrun A, Pilorget H, Samperiz S, Attali T, de Napoli-Cocci S.
Arch Pediatr. 2000;7(6):637-40.
Feingold syndrome is a combination of hand and foot anomalies, microcephaly, tracheo-esophageal fistula, esophageal/duodenal atresia, short palpebral fissures and developmental delay.
9375923
 MIXED_SAMPLE Infant, Newborn
Feingold syndrome: report of a new family and review.
Courtens W, Levi S, Verbelen F, Verloes A, Vamos E.
Am J Med Genet. 1997;73(1):55-60.
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, first reported in 1975 (MIM 164280).
1870095
 MIXED_SAMPLE Infant, Newborn
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.
Brunner HG, Winter RM.
J Med Genet. 1991;28(6):389-94.
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.