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Glucose Transporter Type 1 Deficiency Syndrome 2
A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that is caused by heterozygous mutation in the SLC2A1 gene on chromosome 1p34.
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When to seek help
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Overview
A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that is caused by heterozygous mutation in the SLC2A1 gene on chromosome 1p34.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.