Piebaldism with Neurofibromatosis Type I: A Familial Case
نویسندگان
چکیده
264 Ann Dermatol Received November 22, 2012, Revised April 9, 2013, Accepted for publication April 24, 2013 Corresponding author: Sung Ku Ahn, Department of Dermatology, Yonsei University Wonju College of Medicine, 20 Ilsan-ro, Wonju 220-701, Korea. Tel: 82-33-741-0621, Fax: 82-33-748-2650, E-mail: [email protected] This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http:// creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Fig. 1. The patient presented with depigmented patches and cafe ́-au-lait macules on the abdomen and extremities. (A, B) Hyperpigmented macules were present within the leukodermic patches. (C) He also had the characteristic white forelock. The arrow indicates the white forelock. (D) Multiple cafe ́-au-lait macules and freckling were noted in the axillary areas. The arrow indicates the cafe ́-au-lait macules, while the dotted lines indicate the freckling. http://dx.doi.org/10.5021/ad.2014.26.2.264
منابع مشابه
Piebaldism and Neurofibromatosis type -1: Family Report Familial Case of Piebaldism with Regression of the Depigmentation over the Trunk
Copyright: © 2013 Alembo D. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Piebaldism and Neurofibromatosis type -1: Family Report Familial Case of Piebaldism with Regression of the Depigmentation over the Trunk
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