Omphalocele minor associated with complete absence of the large bowel.

Hdl Handle:
http://hdl.handle.net/10147/207426
Title:
Omphalocele minor associated with complete absence of the large bowel.
Authors:
Ferede, Atakelet; Tareen, Farhan; Gillick, John
Affiliation:
Our Lady's Children's Hospital, Crumlin, Ireland. atakeleta@yahoo.com
Citation:
Pediatr Surg Int. 2009 Jul;25(7):651-3. Epub 2009 Jun 11.
Journal:
Pediatric surgery international
Issue Date:
1-Feb-2012
URI:
http://hdl.handle.net/10147/207426
DOI:
10.1007/s00383-009-2397-8
PubMed ID:
19517123
Abstract:
Colonic atresia, unlike small intestine atresia, is a rare congenital malformation. Congenital absence of the entire colon is exceptionally rare. Moreover, an association of omphalocele and complete absence of the colon has not yet been reported in the literature. We present an infant born with such combination of congenital anomalies.
Language:
eng
MeSH:
*Abnormalities, Multiple; Deafness/complications; Heart Septal Defects, Atrial/complications; Hernia, Umbilical/*complications/*surgery; Humans; Infant, Newborn; Intestinal Atresia/*complications; Intestine, Large/*abnormalities; Male; Parenteral Nutrition, Total; Rare Diseases; Urinary Bladder/abnormalities
ISSN:
1437-9813 (Electronic); 0179-0358 (Linking)

Full metadata record

DC FieldValue Language
dc.contributor.authorFerede, Atakeleten_GB
dc.contributor.authorTareen, Farhanen_GB
dc.contributor.authorGillick, Johnen_GB
dc.date.accessioned2012-02-01T10:24:42Z-
dc.date.available2012-02-01T10:24:42Z-
dc.date.issued2012-02-01T10:24:42Z-
dc.identifier.citationPediatr Surg Int. 2009 Jul;25(7):651-3. Epub 2009 Jun 11.en_GB
dc.identifier.issn1437-9813 (Electronic)en_GB
dc.identifier.issn0179-0358 (Linking)en_GB
dc.identifier.pmid19517123en_GB
dc.identifier.doi10.1007/s00383-009-2397-8en_GB
dc.identifier.urihttp://hdl.handle.net/10147/207426-
dc.description.abstractColonic atresia, unlike small intestine atresia, is a rare congenital malformation. Congenital absence of the entire colon is exceptionally rare. Moreover, an association of omphalocele and complete absence of the colon has not yet been reported in the literature. We present an infant born with such combination of congenital anomalies.en_GB
dc.language.isoengen_GB
dc.subject.mesh*Abnormalities, Multipleen_GB
dc.subject.meshDeafness/complicationsen_GB
dc.subject.meshHeart Septal Defects, Atrial/complicationsen_GB
dc.subject.meshHernia, Umbilical/*complications/*surgeryen_GB
dc.subject.meshHumansen_GB
dc.subject.meshInfant, Newbornen_GB
dc.subject.meshIntestinal Atresia/*complicationsen_GB
dc.subject.meshIntestine, Large/*abnormalitiesen_GB
dc.subject.meshMaleen_GB
dc.subject.meshParenteral Nutrition, Totalen_GB
dc.subject.meshRare Diseasesen_GB
dc.subject.meshUrinary Bladder/abnormalitiesen_GB
dc.titleOmphalocele minor associated with complete absence of the large bowel.en_GB
dc.contributor.departmentOur Lady's Children's Hospital, Crumlin, Ireland. atakeleta@yahoo.comen_GB
dc.identifier.journalPediatric surgery internationalen_GB
dc.description.provinceLeinster-

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