Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990. Disease data Classification Malformation syndrome Synonyms Poikiloderma-alopecia-retrognathism-cleft palate syndrome Poikilodermia - łysienie - retrognatyzm - rozszczep podniebienia ORPHA code 2825 OMIM code 600331 ICD10 code Q87.8 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl