SATB2-associated syndrome due to a chromosomal rearrangement

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Synonyms: 2q33.1 microdeletion syndrome | Del(2)(q33.1) | Monosomy 2q33.1

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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SATB2-associated syndrome due to a chromosomal rearrangement?

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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.

SATB2 Connect

SATB2 Connect will work together with national and international organisations, Australian universities, and medical research institutes to collaborate on awareness, advocacy, and research projects to become a well-supported and informed community to further empower families to ensure they have optimised support necessary for quality of life.

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Clinical Trials

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