PARC syndrome

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Other Names: Poikiloderma, Alopecia, Retrognathism, and Cleft palate

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.

NIH genetic and rare disease info[edit]

PARC syndrome is a rare disease.

Rare and genetic diseases

Rare diseases - PARC syndrome

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