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dc.contributor.authorKutbay, N.I. and Yurekli, B.S. and Yasar, Z. and Akinci, B.
dc.date.accessioned2020-07-02T07:09:52Z
dc.date.available2020-07-02T07:09:52Z
dc.date.issued2019
dc.identifier.citationcited By 0
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85067968643&doi=10.4183%2faeb.2019.129&partnerID=40&md5=7ba5707467b8cfe9a6666dcd65c328dd
dc.identifier.urihttp://hdl.handle.net/20.500.12481/11914
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. © 2019, Acta Endocrinologica Foundation. All rights reserved.
dc.language.isoEnglish
dc.publisherActa Endocrinologica Foundation
dc.titleAn unusual case of acquired partial lipodystrophy presenting with acanthosis nigricans
dc.typeArticle
dc.contributor.departmentCelal Bayar University, Faculty of Medicine, Division of Endocrinology and Metabolism, Manisa, Turkey; Ege University - Endocrinology, Izmir, Turkey; Selahaddin Eyyubi State Hospital, Diyarbakir, Turkey; Dokuz Eylul University - Division of Endocrinology, Izmir, Turkey
dc.identifier.DOI-ID10.4183/aeb.2019.129
dc.identifier.volume15
dc.identifier.pages129-130


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