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Expanding the genotypic and phenotypic spectrum of DYT-TSPOAP1: First report from India
Vikram V Holla1, Debjyoti Dhar1, Riyanka Kumari2
1Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, 560029, India.
Abstract:
Pathogenic variants in TSPOAP1, encoding RIMBP1, cause ultra-rare autosomal recessive dystonia (DYT-TSPOAP1/DYT-22), with only two reports worldwide. Clinical features include upper-segment-predominant dystonia, intellectual disability, eye movement abnormalities, and cerebellar atrophy. We describe two unrelated patients with adolescent-onset generalized dystonia showing cranio-caudal progression due to novel truncating variants in the TSPOAP1 gene.
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