PARC syndrome

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Synonyms: Poikiloderma-alopecia-retrognathism-cleft palate 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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version July 2024

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Clinical Trials

For a list of clinical trials in this disease area, please click here.