Spinocerebellar ataxia type 2 | About the Disease | GARD
网页Spinocerebellar ataxia 2 (SCA2) is a progressive disorder that causes symptoms including uncoordinated movement (ataxia), speech and swallowing difficulties, muscle wasting, slow eye movement, and sometimes dementia.
Spinocerebellar ataxia type 2 - MedlinePlus
网页Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. Explore symptoms, inheritance, genetics of this condition.
Spinocerebellar Ataxia (SCA): Symptoms, Causes & Types - Cleveland Clinic
网页2022年8月29日 — What are the spinocerebellar ataxia types? Experts have discovered more than 40 types of SCAs so far, and that number may increase. They identify types by number (for example, spinocerebellar ataxia type 1, spinocerebellar ataxia type 2 and so on). All types of SCAs have similar causes and symptoms.
Spinocerebellar Ataxia Type 2 - GeneReviews® - NCBI Bookshelf
网页1998年10月23日 — Spinocerebellar ataxia type 2 (SCA2) is characterized by progressive cerebellar ataxia, including nystagmus, slow saccadic eye movements, and in some individuals, ophthalmoparesis or parkinsonism. Pyramidal findings are present; deep tendon reflexes are brisk early on and absent later in the course.
SCA2 - National Ataxia Foundation
网页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 based on geographical location and ethnic background.) Overall, it accounts for about 13 percent of the autosomal dominant Cerebellar Ataxias.
网页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 defects lead to impairment of specific nerve fibers carrying messages to and from the brain resulting in
Spinocerebellar ataxia - Wikipedia
网页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, speech, and eye movements.
Spinocerebellar Ataxia - StatPearls - NCBI Bookshelf
网页2023年9月15日 — Spinocerebellar ataxia (SCA) is an inherited (autosomal dominant), progressive, neurodegenerative, and heterogeneous disease that mainly affects the cerebellum. SCA is a subset of hereditary cerebellar ataxia and is a rare disease.
Spinocerebellar Ataxias including Machado-Joseph Disease
网页Type II—The most common type, generally begins between the ages of about 20 and 50 years of age, has an intermediate rate of progression, and causes various symptoms, including prominent ataxia, spastic gait, and enhanced reflex responses.
Current and emerging treatment modalities for spinocerebellar …
网页BDI-II score significantly decreased in lithium group (p < 0.05). The immediate treatment group demonstrated significantly greater improvements in SARA score in the short-term, especially in truncal ataxia, compared with the delayed-entry treatment group over the 4 weeks (p < 0.001).