A case of Waardenburg syndrome and aganglionosis.

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dc.contributor.authorAritürk E.
dc.contributor.authorTosyali N.
dc.contributor.authorAritürk N.
dc.date.accessioned2024-04-24T18:44:09Z
dc.date.available2024-04-24T18:44:09Z
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.scopus2-s2.0-0026854021
dc.identifier.scopusqualityQ3
dc.identifier.startpage111en_US
dc.identifier.urihttps://hdl.handle.net/11468/24579
dc.identifier.volume34en_US
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.relation.ispartofThe Turkish journal of pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleA case of Waardenburg syndrome and aganglionosis.en_US
dc.titleA case of Waardenburg syndrome and aganglionosis.
dc.typeArticleen_US

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