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pubmed-article:11527200rdf:typepubmed:Citationlld:pubmed
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pubmed-article:11527200pubmed:issue5-6lld:pubmed
pubmed-article:11527200pubmed:dateCreated2001-8-30lld:pubmed
pubmed-article:11527200pubmed:abstractTextOur presentation of four cases demonstrates the essential features of limb-body wall complex (LBWC), representing a compound anomaly pattern in body-wall defects. The diagnosis of this entity is based on two of the three following characteristics: (1) exencephaly/encephalocele and facial clefts; (2) thoraco- and/or abdominoschisis; and (3) limb defects. A definite association with internal anomalies and severe kyphoscoliosis makes a more distinct concept of the pathogenesis reasonable. Limb-body wall malformations result from a malfunction of the ectodermal placodes involving the early embryonic folding process. The poor prognosis of LBWC calls for early antenatal diagnosis.lld:pubmed
pubmed-article:11527200pubmed:languageenglld:pubmed
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pubmed-article:11527200pubmed:issn0179-0358lld:pubmed
pubmed-article:11527200pubmed:authorpubmed-author:SchallerAAlld:pubmed
pubmed-article:11527200pubmed:authorpubmed-author:BernaschekGGlld:pubmed
pubmed-article:11527200pubmed:authorpubmed-author:PumbergerWWlld:pubmed
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pubmed-article:11527200pubmed:volume17lld:pubmed
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pubmed-article:11527200pubmed:pagination486-90lld:pubmed
pubmed-article:11527200pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:11527200pubmed:year2001lld:pubmed
pubmed-article:11527200pubmed:articleTitleLimb-body wall complex: a compound anomaly pattern in body-wall defects.lld:pubmed
pubmed-article:11527200pubmed:affiliationDivision of Paediatric Surgery, University of Vienna, Vienna/Wien, Austria.lld:pubmed
pubmed-article:11527200pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11527200pubmed:publicationTypeCase Reportslld:pubmed