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Acral Peeling Skin Syndrome Resembling Epidermolysis Bullosa Simplex in a 10-Month-Old Boy

The acral peeling skin syndrome (APSS) is a rare autosomal recessive disorder clinically characterized by asymptomatic desquamation of the skin limited to the hands and feet and histologically by cleavage at the stratum granulosum and stratum corneum level [Kiritsi et al.: J Invest Dermatol 2010;130...

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Main Authors: S. Kavaklieva, I. Yordanova, L. Bruckner-Tuderman, C. Has
Format: Artigo
Language:Inglês
Published: Karger Publishers 2013-08-01
Series:Case Reports in Dermatology
Subjects:
Acral peeling skin syndrome
TGM5 gene
CSTA gene
Online Access:http://www.karger.com/Article/FullText/354572
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