A Case Report of Allgrove Syndrome with Neurological Involvement

dc.contributor.authorTuzcu, Alpaslan Kemal
dc.contributor.authorSoylu, Hikmet
dc.contributor.authorKılınç, Faruk
dc.contributor.authorTuna, Mazhar Müslüm
dc.contributor.authorAteş, Kenan
dc.contributor.authorPekkolay, Zafer
dc.date.accessioned2024-04-24T19:07:30Z
dc.date.available2024-04-24T19:07:30Z
dc.date.issued2015
dc.departmentDicle Üniversitesien_US
dc.description.abstractAllgrove syndrome is a very rare seen disorder with an autosomal recessive trait. The three characteristics of disease are alacrima, achalasia and adrenal failure. Alacrimia is the first manifestation in most cases. Achalasia and adrenal failure are seen later. Neurological involvement is rare and usually occurs in older age. A woman 22 years old admitted to our hospital with adrenal failure crisis. She had alacrimia and used teardrop for many years. Achalasia was diagnosed after evaluation of her dysphagia. Thus, diagnosis of Allgrove syndrome was done. Autonomic cardiac dysfunction and peripheral motor neuropathy were detected. In conclusion, Allgrove syndrome is rare and has life threatening potential due to adrenal failure. Early diagnosis and appropriate treatment may improve life quality and expectancy. Patients with relevant symptoms should be evaluated for autonomic neuropathyen_US
dc.identifier.endpage2574en_US
dc.identifier.issn2147-0634
dc.identifier.issue3en_US
dc.identifier.startpage2570en_US
dc.identifier.trdizinid230427
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/230427
dc.identifier.urihttps://hdl.handle.net/11468/27416
dc.identifier.volume4en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofMedicine Science
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA Case Report of Allgrove Syndrome with Neurological Involvementen_US
dc.titleA Case Report of Allgrove Syndrome with Neurological Involvement
dc.typeArticleen_US

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