Acral Peeling Skin Syndrome: A Case of Two Brothers
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2009.00917.x/fullpdf
Reference11 articles.
1. Acral peeling skin syndrome;Shwayder;Arch Dermatol,1997
2. Acral peeling skin syndrome;Hashimoto;J Am Acad Dermatol,2000
3. Peeling skin syndrome with aminoaciduria;Inamadar;Pediatr Dermatol,2005
4. A homozygous missense mutation in tgm5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome;Cassidy;Am J Hum Genet,2005
5. The peeling skin syndrome;Levy;J Am Acad Dermatol,1982
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1. Hereditary Disorders of Cornification;Hurwitz Clinical Pediatric Dermatology;2016
2. Rarely occurring genodermatosis (acral peeling skin syndrome) – case report. Literature review of localized and generalized variants;Dermatology Review;2015
3. Lifelong Desquamation of the Hands and Feet;JAMA Dermatology;2014-06-01
4. Keratolysis exfoliativa (dyshidrosis lamellosa sicca): a distinct peeling entity;British Journal of Dermatology;2012-10-05
5. Localized Exfoliating Rash with Paresthesia Possibly Due to Clonazepam;Journal of Child and Adolescent Psychopharmacology;2012-08
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