Parkinsonism & Related Disorders, Год журнала: 2025, Номер unknown, С. 107850 - 107850
Опубликована: Апрель 1, 2025
Язык: Английский
Parkinsonism & Related Disorders, Год журнала: 2025, Номер unknown, С. 107850 - 107850
Опубликована: Апрель 1, 2025
Язык: Английский
Journal of Neural Transmission, Год журнала: 2025, Номер unknown
Опубликована: Апрель 17, 2025
Abstract Although α-synuclein pathology is typically associated with Lewy body diseases and multiple systems atrophy, increasing evidence indicates that it also occurs in a group of lysosomal storage disorders termed sphingolipidoses caused by the incomplete degradation, subsequent accumulation, class lipids sphingolipids. Notably, number genes cause are risk for diseases, suggesting aetiological links between these distinct disorders. In present review, we discuss which has been reported: Gaucher disease, Krabbe metachromatic leukodystrophy, Tay-Sachs disease Anderson-Fabry describe characteristic clinical pathological features disorders, addition to Finally, evaluate mechanisms underlie rare particular attention how enzymatic deficiency, substrate or both, could contribute genesis implications this diseases.
Язык: Английский
Процитировано
0Parkinsonism & Related Disorders, Год журнала: 2025, Номер unknown, С. 107850 - 107850
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0