The association of common atrium with smith-lemli-opitz syndrome in an infant

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dc.contributor.authorSert A.
dc.contributor.authorPirgon Ö.
dc.contributor.authorAtabek M.E.
dc.contributor.authorDogan M.
dc.date.accessioned2020-03-26T17:29:09Z
dc.date.available2020-03-26T17:29:09Z
dc.date.issued2008
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractSmith-Lemli-Opitz syndrome is a rare syndrome presenting with multiple congenital anomalies/mental retardation associated with low plasma cholesterol levels. The spectrum of severity extends from prenatal death with holoprosencephaly or other lethal malformations, to patients with minimal physical abnormalities and normal intelligence or minimal intellectual impairment. Congenital heart defect is found in half of the Smith-Lemli-Opitz syndrome patients. To our knowledge, the association of common atrium and Smith-Lemli-Opitz syndrome has not been described before in the medical literature. We present a 4-month-old infant case of such association.en_US
dc.identifier.endpage264en_US
dc.identifier.issn1019-1941en_US
dc.identifier.issue3en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage261en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/22918
dc.identifier.volume21en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofMarmara Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectCommon atriumen_US
dc.subjectInfanten_US
dc.subjectSmith-Lemli-Opitz syndromeen_US
dc.titleThe association of common atrium with smith-lemli-opitz syndrome in an infanten_US
dc.typeArticleen_US

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