Painless erosions on the hands and feet of a 7‐year‐old boy
Author:
Affiliation:
1. Cooper Medical School of Rowan University Camden NJ USA
2. Cooper University Hospital Camden NJ USA
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/pde.14082
Reference9 articles.
1. Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome
2. Acral Peeling Skin Syndrome with TGM5 Gene Mutations May Resemble Epidermolysis Bullosa Simplex in Young Individuals
3. Acral peeling skin syndrome
4. A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome
5. TGM5 Mutations Impact Epidermal Differentiation in Acral Peeling Skin Syndrome
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