AN UNUSUAL CASE OF ACQUIRED PARTIAL LIPODYSTROPHY PRESENTING WITH ACANTHOSIS NIGRICANS

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dc.contributor.authorKutbay, N. Ozdemir
dc.contributor.authorYurekli, B. Sarer
dc.contributor.authorYasar, Z.
dc.contributor.authorAkinci, B.
dc.date.accessioned2019-10-27T09:48:00Z
dc.date.available2019-10-27T09:48:00Z
dc.date.issued2019
dc.departmentEge Üniversitesien_US
dc.description.abstractAbout 250 patients with acquired partial lipodystrophy (Barraquer-Simons) syndrome have been reported so far. It is characterized by the loss of adipose tissue from the face and upper extremities, and accumulated fat in the rest of the body. The disease usually starts in females during childhood or adolescence, and usually after a febrile illness. Fat loss often comes into view in months or years. We present a 23-year-old female patient with acquired partial lipodystrophy, which is rarely seen.en_US
dc.identifier.doi10.4183/aeb.2019.129en_US
dc.identifier.endpage130en_US
dc.identifier.issn1841-0987
dc.identifier.issn1843-066X
dc.identifier.issue1en_US
dc.identifier.pmid31149072en_US
dc.identifier.startpage129en_US
dc.identifier.urihttps://doi.org/10.4183/aeb.2019.129
dc.identifier.urihttps://hdl.handle.net/11454/29471
dc.identifier.volume15en_US
dc.identifier.wosWOS:000470035300020en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherEditura Acad Romaneen_US
dc.relation.ispartofActa Endocrinologica-Bucharesten_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcquired partial lipodystrophyen_US
dc.subjectinsulin resistanceen_US
dc.subjectdiabetesen_US
dc.titleAN UNUSUAL CASE OF ACQUIRED PARTIAL LIPODYSTROPHY PRESENTING WITH ACANTHOSIS NIGRICANSen_US
dc.typeLetteren_US

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