alexa Piebaldism Associated with Neurofibromatosis Type I: A Case Report
ISSN: 2155-9554

Journal of Clinical & Experimental Dermatology Research
Open Access

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Case Report

Piebaldism Associated with Neurofibromatosis Type I: A Case Report

Ayman Elgendy1*, Eslam Alshawadfy2*, Eman Ali2* and Abdelaziz Altaweel1*

1Department of Dermatology, Benha University, Egypt

2Department of Dermatology research, National Research Centre, Cairo, Egypt

*Corresponding Authors:
Ayman Elgendy
Professor of Dermatology and
Venereology, Benha University, Egypt
Tel: +966507364687
Email: [email protected]

Eslam Alshawadfy
Ass. Lecturer of Dermatology and
Venereology (National Research Centre
Cairo, Egypt), MSc. Dermatology, MRCP (SCE Dermatology)
European Board of Dermatology& Venereology (Frankfurt)
Diploma in Dermatology (RCPSG) Glasgow.
Tel: +201150177887
Email: [email protected]

Eman Ali
Ass. Lecturer of Dermatology and
Venereology (National Research Centre
Cairo, Egypt), MSc. Dermatology
American Board of Aesthetic Medicine
Tel: +201005250969
Email: [email protected]

Abdelaziz Altaweel
Professor of Dermatology and Venereology,
Benha University, Egypt
Tel: +201001633773
Email: [email protected]

Received Date: March 12, 2015, Accepted Date: March 28, 2015, Published Date:March 30, 2015

Citation: Elgendy A, Alshawadfy E, Ali E, Altaweel A (2015) Piebaldism Associated with Neurofibromatosis Type I: A Case Report. J Clin Exp Dermatol Res 6:274. doi: 10.4172/2155-9554.1000274

Copyright: © 2015 Elgendy A, et al. 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.

 

Abstract

Piebaldism is a rare disorder present at birth and inherited as an autosomal dominant trait. It results from a mutation in the c-kit proto-oncogene and is associated with a defect in the migration and differentiation of melanoblasts from the neural crest. We report a 15-year-old girl with both piebaldism and neurofibromatosis type 1 (NF1). She presented with a congenital depigmented patch of the forehead, as well as acquired white forelock, depigmentation of the medial eyebrows, and depigmented patches of the legs. In addition, some café au lait macules were observed at birth on the trunk and neck. To our knowledge, the association of piebaldism and NF1 has been described previously in at least 6 case reports. Awareness of this rare association is relevant to ensure early diagnosis and adequate follow-up for NF1.

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