PARC syndrome
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 source]
PARC syndrome is a rare disease.
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