Craniofacial conodysplasia

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Craniofacial conodysplasia

Craniofacial conodysplasia is characterised by craniofacial dysplasia cone-shaped physes of the hands and feet and neurological manifestations resembling cerebral palsy. It has been described in one family. The syndrome appeared to be transmitted as a dominant trait.

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 April 2024

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Craniofacial conodysplasia?

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