Charlie M syndrome

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Charlie M syndrome

A rare multiple congenital anomalies/dysmorphic syndrome characterized by the common manifestations found in oromandibular-limb hypogenesis syndromes(OLHS) group such as hypoplasia of the mandible variable limb anomalies like syndactylyl and ectrodactyly small mouth cleft palate and hypodontia accompanied by other clinical signs such as facial paralysis facial asymmetry hypertelorism hypoglossia/aglossia absent or conically crowned incisors and ectromelia. There have been no further descriptions in the literature since 1976.

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 February 2024

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