A familial case of spinocerebellar attack type I. Clinical and diagnostic parallels
Spinocerebellar ataxia is a neurodegenerative disease with an autosomal dominant type of inheritance, rapid progression of clinical manifestations with onset at a young age. The clinical case of a 34-year-old patient with spinocerebellar ataxia type I, burdened by a hereditary history and the formation of the anticipation phenomenon, is considered. It was noted thatclinical symptoms preceded neuroimaging data.
Authors
- Д. И. Созаева (ORCID: https://orcid.org/0000-0002-3941-5540)
- A. M. Domracheva (ORCID: https://orcid.org/0009-0009-4402-1157)
- N. A. Fomina-Chertousova (ORCID: https://orcid.org/0000-0003-4246-2097)
- E. S. Pivacheva
Institutions
- Rostov State Medical University (RU)
- Central Clinical Hospital No 2 named Semashko (RU)
Publication Details
- Journal
- South Russian Journal of Therapeutic Practice
- Published
- 2025-02-04
- DOI
- https://doi.org/10.21886/2712-8156-2025-6-1-88-94
- Citations
- 1
- Primary Topic
- Neurological and metabolic disorders
- Type
- article
- Field-Weighted Citation Impact
- 1.29