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Up to: Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
PARC syndrome
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.
This condition has no sub-types.