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Peeling skin syndrome

ORPHA:817

Definition

A group of rare autosomal recessive forms of ichthyosis clinically characterized by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution for generalized PSS type A (noninflammatory) or B (inflammatory).

Prevalence
Unknown
Inheritance
Autosomal recessive
Age of onset
Infancy, Neonatal