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Birt-Hogg-Dube Syndrome

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dc.contributor.authorEMİROĞLU, Nazan
dc.contributor.authorCENGİZ, Fatma Pelin
dc.contributor.authorTOSUNER, ZEYNEP
dc.contributor.authorBAHALI, ANIL GÜLSEL
dc.contributor.authorONSUN, Nahide
dc.contributor.institutionauthorEMİROĞLU, NAZAN
dc.contributor.institutionauthorCENGİZ, FATMA PELIN
dc.contributor.institutionauthorTOSUNER, ZEYNEP
dc.contributor.institutionauthorBAHALI, ANIL GÜLSEL
dc.contributor.institutionauthorONSUN, NAHIDE
dc.date.accessioned2020-10-22T18:11:15Z
dc.date.available2020-10-22T18:11:15Z
dc.date.issued2018-07-01T00:00:00Z
dc.description.abstractBirt-Hogg-Dube syndrome is characterized by cutaneous findings, including fibrofolliculomas, angiofibromas, fibroepithelial polyps, and trichodiscomas. It is an inherited autosomal dominant disorder. This syndrome also includes extra-cutaneous findings, such as pulmonary cysts, spontaneous pneumothorax, and renal cancer. Because of the systemic involvement, early diagnosis and treatment are important. Here, we report the case of a 53-year-old man diagnosed as having Birt-Hogg-Dube syndrome.
dc.identifier.citationEMİROĞLU N., CENGİZ F. P. , TOSUNER Z., BAHALI A. G. , ONSUN N., -Birt-Hogg-Dube Syndrome-, BEZMIALEM SCIENCE, cilt.6, ss.220-222, 2018
dc.identifier.doi10.14235/bs.2017.1453
dc.identifier.trdizintrdizin
dc.identifier.urihttp://hdl.handle.net/20.500.12645/24016
dc.identifier.wosWOS:000446222000014
dc.titleBirt-Hogg-Dube Syndrome
dc.typeArticle
dspace.entity.typePublication
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local.publication.goal03 - Sağlık ve Kaliteli Yaşam
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