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A rare case of acquired partial lipodystrophy (Barraquer-Simons syndrome) with localized scleroderma

2013; Wiley; Volume: 53; Issue: 1 Linguagem: Inglês

10.1111/j.1365-4632.2011.05435.x

1365-4632

Kittisak Payapvipapong, Nucha Niumpradit, Artit Nakakes, Kitti Buranawuti,

Erythrocyte Function and Pathophysiology

International Journal of DermatologyVolume 53, Issue 1 p. 82-84 Case report A rare case of acquired partial lipodystrophy (Barraquer–Simons syndrome) with localized scleroderma Kittisak Payapvipapong MD, Kittisak Payapvipapong MD Division of Dermatology, and Division ofSearch for more papers by this authorNucha Niumpradit MD, Nucha Niumpradit MD Division of Dermatology, and Division ofSearch for more papers by this authorArtit Nakakes MD, Artit Nakakes MD Division of Dermatology, and Division ofSearch for more papers by this authorKitti Buranawuti MD, FACMG, Kitti Buranawuti MD, FACMG Medical Genetics, Department of Medicine, Phramongkutklao Hospital, Bangkok, ThailandSearch for more papers by this author Kittisak Payapvipapong MD, Kittisak Payapvipapong MD Division of Dermatology, and Division ofSearch for more papers by this authorNucha Niumpradit MD, Nucha Niumpradit MD Division of Dermatology, and Division ofSearch for more papers by this authorArtit Nakakes MD, Artit Nakakes MD Division of Dermatology, and Division ofSearch for more papers by this authorKitti Buranawuti MD, FACMG, Kitti Buranawuti MD, FACMG Medical Genetics, Department of Medicine, Phramongkutklao Hospital, Bangkok, ThailandSearch for more papers by this author First published: 15 May 2013 https://doi.org/10.1111/j.1365-4632.2011.05435.xCitations: 4 Kittisak Payapvipapong, MD Phramongkutklao Hospital 315 Ratchavithi ST Bangkok Thailand E-mail: [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL References 1Garg A. Acquired and inherited lipodystropies. N Engl J Med2004; 350: 1220– 1234. 2Misra A, Peethambaram A, Garg A. Clinical features and metabolic and autoimmune derangements in acquired partial lipodystropy: report of 35 cases and review of the literature. Medicine2004; 83: 18– 34. 3Walport MJ, Davies KA, Botto M, et al. C3 nephritic factor and SLE: report of four cases and review of the literature. QJM1994; 87: 609– 615. 4Capeau J, Magre J, Caron-Debarle M, et al. Human lipodystrophies: genetic and acquired disease of adipose tissue. Endocr Dev2010; 19: 1– 20. 5Hegele RA, Cao H, Li DM, et al. Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy. Am J Hum Genet2006; 79: 383– 389. 6Biasi D, Caramasci P, Carletto A, et al. A case of acquired partial lipodystropy associated with localized scleroderma and undifferentiated connective tissue disease. Rheumatol Int1999; 19: 75– 76. Citing Literature Volume53, Issue1January 2014Pages 82-84 ReferencesRelatedInformation