Steatocystoma multiplex - case report
Abstract
Keywords
Full Text:
PDFReferences
Covello SP, Smith FJ, Sillevis Smitt JH et al: Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. Br J Dermatol, 1998, 139 (3):475–80.
Riedel C, Brinkmeier T, Kutzne H, Plewig G, Frosch PJ: Late onset of a facial variant of steatocystoma multiplex—calretinin as a specific marker of the follicular companion cell layer. J Dtsch Dermatol Ges, 2008, 6(6):480–2.
Kamra HT, Gadgil PA, Ovhal AG, Narkhede RR: Steatocystoma multiplex-a rare genetic disorder: a case report and review of the literature. J Clin Diagn Res, 2013, 7(1):166-8.
Kim SJ, Park HJ, Oh ST, Lee JY, Cho BK. A case of steatocystoma multiplex limited to scalp. Ann Dermatol, 2009; 21(1):106–09.
Yanagi T, Matsumura T: Steatocystoma multi-plex presenting as acral subcutaneous nodules. Acta Derm Venereol, 2006, 86(4):374–5.
Park KY, Oh KK, Noh TW: Steatocystoma multiplex: Mammographic and sonographic manifestations. AJR, 2003, 180:27.
Kamra HT, Gadgil PA, Ovhal AG, Narkhede RR.: Steatocystoma multiplex-a rare genetic disorder: a case report and review of the literature. J Clin Diagn Res, 2013, 7(1):166-8.
DOI: http://dx.doi.org/10.22551/2014.01.0101.10008
Copyright (c)
Archive of Clinical Cases is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
ISSN: 2360-6975