Diabetic Ketoacidosis, Thyroiditis and Alopecia Areata in a Child with Down Syndrome

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dc.contributor.authorPirgon, Ozgur
dc.contributor.authorAtabek, Mehmet Emre
dc.contributor.authorSert, Ahmet
dc.date.accessioned2020-03-26T17:38:15Z
dc.date.available2020-03-26T17:38:15Z
dc.date.issued2009
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractA 10-year-old girl with Down syndrome and alopecia areata was admitted with severe ketoacidosis. She had high blood glucose level: 615 mg/dL and her HbAlc level was 13.3 %. After the control of ketoacidosis and reduction of the plasma glucose level, we found low free T4 level and high TSH levels. Thyroid peroxidase antibodies titer was 1383 IU/mL and both gliadin and endomysial antibodies were negative. This was the first report of a child with Down syndrome showing type 1 diabetes combined with alopecia areata and autoimmune thyroid disease. [Indian J Pediatr 2009; 76 (12) : 1263-1264] E-mail: ozpirgon@hotmail.comen_US
dc.identifier.doi10.1007/s12098-009-0242-7en_US
dc.identifier.endpage1264en_US
dc.identifier.issn0019-5456en_US
dc.identifier.issn0973-7693en_US
dc.identifier.issue12en_US
dc.identifier.pmid20012788en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage1263en_US
dc.identifier.urihttps://dx.doi.org/10.1007/s12098-009-0242-7
dc.identifier.urihttps://hdl.handle.net/20.500.12395/23420
dc.identifier.volume76en_US
dc.identifier.wosWOS:000274246400011en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSPRINGER INDIAen_US
dc.relation.ispartofINDIAN JOURNAL OF PEDIATRICSen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectDown syndromeen_US
dc.subjectDiabetic ketoacidosisen_US
dc.subjectThyroiditisen_US
dc.subjectAlopeciaen_US
dc.titleDiabetic Ketoacidosis, Thyroiditis and Alopecia Areata in a Child with Down Syndromeen_US
dc.typeArticleen_US

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