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Updated: Aug 30, 2026

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Published on: September 12, 2020
Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation
Yoshiki Sekijima1, Takao Hashimoto, Osam Onodera
1Third Department of Medicine, Shinshu University School of Medicine, Asahi, Matsumoto, Japan.
Abstract:
A 14-year-old girl, homozygous for an insertion mutation of aprataxin (APTX), 689 ins T, is described. She presented with severe generalized dystonia, ataxia, ocular motor apraxia, and areflexia. The dystonia of this patient suggests involvement of the basal ganglia or thalamus, along with clinical diversity in this disorder.
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