Peeling Skin Syndrome (PSS)

Peeling Skin Syndrome, also known as familial continuous skin peeling syndrome, is related to peeling skin syndrome 2 and peeling skin syndrome 1. An important gene associated with Peeling Skin Syndrome is FLG2 (Filaggrin 2), and among its related pathways/superpathways are Nervous system development and Keratinization. The drugs Heparin, bovine and Latanoprost have been mentioned in the context of this disorder. Affiliated tissues include skin and eye, and related phenotype is integument.