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- W2079665128 abstract "Abstract Peeling skin syndrome is an extremely rare genodermatosis of possible autosomal recessive inheritance, characterized by asymptomatic spontaneous exfoliation of the stratum corneum at a subcorneal or intracorneal level. It usually presents at birth or appears later in early childhood. The condition may be generalized or localized. Here we describe a case of localized continual skin peeling limited to the facial skin in a 6‐month‐old infant, with two other members of the family affected with the same condition. A few cases of localized skin peeling limited to the acral surfaces have been described in the literature, but a familial case of localized skin peeling limited to the facial skin has not been described before. We believe that our patient represents a new subtype of peeling skin syndrome, limited to the skin of the face." @default.
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- W2079665128 date "2007-03-01" @default.
- W2079665128 modified "2023-10-16" @default.
- W2079665128 title "Facial peeling skin syndrome: A case report and a brief review" @default.
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- W2079665128 doi "https://doi.org/10.1111/j.1365-4632.2006.03074.x" @default.
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