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Dystonia 22, Juvenile-Onset
A dystonia characterized by progressive, generalized dystonia associated with cognitive decline and cerebellar atrophy on brain imaging that is caused by homozygous loss-of-function mutation in the TSPOAP1 gene (610764)
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When to seek help
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Overview
A dystonia characterized by progressive, generalized dystonia associated with cognitive decline and cerebellar atrophy on brain imaging that is caused by homozygous loss-of-function mutation in the TSPOAP1 gene (610764)
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.