Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait and is often associated with poor coordination of hands, …

SCA2 is one of the more common types of Spinocerebellar Ataxias. SCA2 is about twice as common as SCA1 which appears in approximately 1 to 2 people in 100,000. (The ratio varies …

Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. Explore symptoms, inheritance, genetics of this condition.

Spinocerebellar ataxia (SCA) comprises more than 40 types of similar inherited brain disorders. SCA affects your cerebellum, a part of your brain vital to physical movement. It causes …

2024年7月19日 · SCA2 (also known as olivopontocerebellar atrophy) involves vision problems, eye muscle control, and degeneration of the retina (the light-sensing part of the eye). …

Spinocerebellar ataxia 2 (SCA2) is a progressive disorder that causes symptoms including uncoordinated movement (ataxia), speech and swallowing difficulties, muscle wasting, slow …

2023年9月15日 · Spinocerebellar ataxia (SCA) is a progressive neurodegenerative inherited (autosomal dominant) heterogeneous disease that mainly affects the cerebellum. SCA is a …

What is spinocerebellar Ataxia type 2? Spinocerebellar Ataxia type 2 (SCA12) is one specific type of Ataxia among a group of inherited diseases of the central nervous system. In SCA2, genetic …

Spinocerebellar ataxia type 2 (SCA2) represents a genetic disorder with an autosomal dominant inheritance caused by a CAG expansion in the ubiquitously expressed ATXN2 gene encoding …

Spinocerebellar ataxia type 2 (SCA2) is one type of ataxia among a group of inherited diseases of the central nervous system. In SCA2, genetic defects lead to impairment of specific nerve …