Familial congenital mirror movements

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Synonyms: Familial congenital controlateral synkinesia | Hereditary congenital controlateral synkinesia | Hereditary congenital mirror movements | Isolated congenital controlateral synkinesia | Isolated congenital mirror movements

A rare genetic movement disorder characterized by involuntary movements on one side of the body that mirror intentional movements on the opposite side of the body which are present in various first-degree members of a family persist beyond the first decade of life and have no associated comorbidities.

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 July 2024

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Familial congenital mirror movements?

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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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