PARC syndrome

MONDO:0010867

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, poikiloderma, alopecia, retrognathism, and cleft palate

0 clinical trials for this condition and its sub-types, 0 tagged with PARC syndrome itself.

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Part of

↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163)

Including sub-types (0) Tagged with PARC syndrome (0)

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