Catel-Manzke syndrome

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Synonyms: Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome | Index finger anomaly-Pierre Robin syndrome | Micrognathia digital syndrome | Palatodigital syndrome, Catel-Manzke type | Pierre Robin sequence-hyperphalangy-clinodactyly syndrome | Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome

Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia cleft palate and glossoptosis.

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 http://www.orphadata.org. Data version June 2024

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Catel-Manzke syndrome?

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Advocacy Organizations

Project CASK

VISION Project CASK believes in a world free of the life limitations and debilitating effects of CASK gene disorders. ​MISSION To accelerate breakthroughs in research to develop treatments and a cure for CASK gene disorders. ​VALUES Collaboration. Transparency. Urgency.

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Clinical Trials

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