Familial and genetic aspects of neuronal intestinal dysplasia and Hirschsprung's disease

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dc.contributor.authorMoore S.W.
dc.contributor.authorKaschula R.O.C.
dc.contributor.authorCywes S.
dc.date.accessioned2011-05-15T16:17:43Z
dc.date.available2011-05-15T16:17:43Z
dc.date.issued1993
dc.description.abstractA familial occurrence of Hirschsprung's disease and neuronal intestinal dysplasia (NID) is reported. Familial occurrence of NID in a parent and long-segment Hirschsprung's disease in two children in a family as well as a further report of NID in monozygotic twins is described. The linkage of these neurodevelopmental conditions is explored and a common etiologic mechanism for the two conditions is postulated.
dc.description.versionArticle
dc.identifier.citationPediatric Surgery International
dc.identifier.citation8
dc.identifier.citation5
dc.identifier.issn01790358
dc.identifier.urihttp://hdl.handle.net/10019.1/14344
dc.subjectadult
dc.subjectarticle
dc.subjectcase report
dc.subjectdysplasia
dc.subjectfamilial disease
dc.subjectfamily history
dc.subjectfemale
dc.subjectgenetic association
dc.subjecthirschsprung disease
dc.subjecthuman
dc.subjectinfant
dc.subjectintestine malformation
dc.subjectmale
dc.subjectmonozygotic twins
dc.titleFamilial and genetic aspects of neuronal intestinal dysplasia and Hirschsprung's disease
dc.typeArticle
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