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dc.contributor.authorKilicli, Fatih
dc.contributor.authorAcibucu, Fettah
dc.contributor.authorSenel, Soner
dc.contributor.authorDokmetas, Hatice Sebila
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:03:45Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:03:45Z
dc.date.issued2012
dc.identifier.issn0037-5675
dc.identifier.urihttps://hdl.handle.net/20.500.12418/9141
dc.descriptionWOS: 000305002200003en_US
dc.descriptionPubMed ID: 22584989en_US
dc.description.abstractAllgrove syndrome is a rare autosomal recessive disorder. It is also known as the 3A syndrome and characterised by the triad of achalasia, alacrima and adrenal insufficiency. The AAAS gene is encoded on chromosome 12q13. We report the case of a 23-year-old woman who presented at the hospital with adrenal crisis that was triggered by infection of the urinary system and gastrointestinal bleeding. She had a known diagnosis of achalasia for eight years, and ophthalmologic examination revealed alacrima. Based on our findings, the patient was diagnosed with Allgrove syndrome.en_US
dc.language.isoengen_US
dc.publisherSINGAPORE MEDICAL ASSOCen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectadrenal insufficiencyen_US
dc.subjectachalasiaen_US
dc.subjectalacrimaen_US
dc.subjectAllgrove syndromeen_US
dc.titleAllgrove syndromeen_US
dc.typearticleen_US
dc.relation.journalSINGAPORE MEDICAL JOURNALen_US
dc.contributor.department[Dokmetas, Hatice Sebila] Cumhuriyet Univ, Fac Med, Dept Endocrinol & Metab, Sivas, Turkey -- [Senel, Soner] Cumhuriyet Univ, Dept Rheumatol, Sivas, Turkeyen_US
dc.identifier.volume53en_US
dc.identifier.issue5en_US
dc.identifier.endpageE94en_US
dc.identifier.startpageE92en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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