학술논문
Genetics Corner: Familial Duodenal Atresia Due to Feingold Syndrome.
Document Type
Article
Author
Source
Subject
*ECHOCARDIOGRAPHY
*ENTEROSTOMY
*MULTIPLE human abnormalities
*ATRIAL septal defects
*INTESTINAL diseases
*ABDOMINAL surgery
*DUODENAL obstructions
*GENE mapping
DIGESTIVE organ abnormalities
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Language
ISSN
1932-7129
Abstract
A case study is presentedin which a genetic consultation was requested for a female preterm patient with familial history of duodenal atresia. The patient was diagnosed with autosomal dominant Feingold Syndrome confirmed by genetic testing of her mother, Duodenal atresia is usually sporadic, although it can also be reported with genetic and chromosomal syndromes.