PARC syndrome

PARC syndrome

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.

Also known as PARC syndrome, poikiloderma-alopecia-retrognathism-cleft palate syndrome — per MONDO

Also identified as