Familial combined duodenal and jejunal atresia
Combined duodenal and jejunal atresia is extremely uncommon. The familial occurrence of congenital duodenal and small bowel atresia is even more unusual. To the authors' knowledge, this is the first report of two siblings with simultaneous duodenal and jejunal atresia who underwent successful s...
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Veröffentlicht in: | Journal of pediatric surgery 1996-11, Vol.31 (11), p.1573-1573 |
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container_title | Journal of pediatric surgery |
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creator | Gross, E Armon, Y Abu-Dalu, K Gale, R Schiller, M |
description | Combined duodenal and jejunal atresia is extremely uncommon. The familial occurrence of congenital duodenal and small bowel atresia is even more unusual. To the authors' knowledge, this is the first report of two siblings with simultaneous duodenal and jejunal atresia who underwent successful surgical repair. The report may support the genetic origin of some forms of high intestinal atresia. |
doi_str_mv | 10.1016/S0022-3468(96)90182-7 |
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The familial occurrence of congenital duodenal and small bowel atresia is even more unusual. To the authors' knowledge, this is the first report of two siblings with simultaneous duodenal and jejunal atresia who underwent successful surgical repair. The report may support the genetic origin of some forms of high intestinal atresia.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/S0022-3468(96)90182-7</identifier><identifier>PMID: 8943127</identifier><identifier>CODEN: JPDSA3</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Abnormalities, Multiple - surgery ; Biological and medical sciences ; Duodenal Obstruction - congenital ; Duodenal Obstruction - surgery ; Family Health ; Humans ; Infant, Newborn ; Intestinal Atresia - surgery ; Jejunum - abnormalities ; Jejunum - surgery ; Male ; Medical sciences ; Stomach, duodenum, intestine, rectum, anus ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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The familial occurrence of congenital duodenal and small bowel atresia is even more unusual. To the authors' knowledge, this is the first report of two siblings with simultaneous duodenal and jejunal atresia who underwent successful surgical repair. The report may support the genetic origin of some forms of high intestinal atresia.</description><subject>Abnormalities, Multiple - surgery</subject><subject>Biological and medical sciences</subject><subject>Duodenal Obstruction - congenital</subject><subject>Duodenal Obstruction - surgery</subject><subject>Family Health</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Intestinal Atresia - surgery</subject><subject>Jejunum - abnormalities</subject><subject>Jejunum - surgery</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Stomach, duodenum, intestine, rectum, anus</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gross, E</creatorcontrib><creatorcontrib>Armon, Y</creatorcontrib><creatorcontrib>Abu-Dalu, K</creatorcontrib><creatorcontrib>Gale, R</creatorcontrib><creatorcontrib>Schiller, M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gross, E</au><au>Armon, Y</au><au>Abu-Dalu, K</au><au>Gale, R</au><au>Schiller, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Familial combined duodenal and jejunal atresia</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>1996-11-01</date><risdate>1996</risdate><volume>31</volume><issue>11</issue><spage>1573</spage><epage>1573</epage><pages>1573-1573</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><coden>JPDSA3</coden><abstract>Combined duodenal and jejunal atresia is extremely uncommon. The familial occurrence of congenital duodenal and small bowel atresia is even more unusual. To the authors' knowledge, this is the first report of two siblings with simultaneous duodenal and jejunal atresia who underwent successful surgical repair. The report may support the genetic origin of some forms of high intestinal atresia.</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>8943127</pmid><doi>10.1016/S0022-3468(96)90182-7</doi><tpages>1</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE |
subjects | Abnormalities, Multiple - surgery Biological and medical sciences Duodenal Obstruction - congenital Duodenal Obstruction - surgery Family Health Humans Infant, Newborn Intestinal Atresia - surgery Jejunum - abnormalities Jejunum - surgery Male Medical sciences Stomach, duodenum, intestine, rectum, anus Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system |
title | Familial combined duodenal and jejunal atresia |
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