A CASE OF WAARDENBURG SYNDROME AND AGANGLIONOSIS

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dc.contributor.authorARITURK, E
dc.contributor.authorTOSYALI, N
dc.contributor.authorARITURK, N
dc.date.accessioned2024-04-24T17:44:37Z
dc.date.available2024-04-24T17:44:37Z
dc.date.issued1992
dc.departmentDicle Üniversitesien_US
dc.description.abstractWaardenburg's syndrome is characterized by a broad nasal root, pigmentation disturbance and congenital deafness while aganglionosis is described as the partial or complete lack of ganglion cells in the alimentary tract. This report describes a five-day-old male infant with Waardenburg's Syndrome associated with total aganglionosis of the colon, ileum and distal jejunum and draws attention to the causal relationship between these two entities.en_US
dc.identifier.endpage114en_US
dc.identifier.issn0041-4301
dc.identifier.issue2en_US
dc.identifier.pmid1440950
dc.identifier.startpage111en_US
dc.identifier.urihttps://hdl.handle.net/11468/22189
dc.identifier.volume34en_US
dc.identifier.wosWOS:A1992JL48600008
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherTurkish J Pediatricsen_US
dc.relation.ispartofTurkish Journal of Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectWaardenburg Syndromeen_US
dc.subjectHirschsprungs Diseaseen_US
dc.subjectNeural Cresten_US
dc.titleA CASE OF WAARDENBURG SYNDROME AND AGANGLIONOSISen_US
dc.titleA CASE OF WAARDENBURG SYNDROME AND AGANGLIONOSIS
dc.typeArticleen_US

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