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Spinocerebellar Ataxia Type 2 - GeneReviews® - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/NBK1275/
webOct 23, 1998 · 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.
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Ataxia - Symptoms and causes - Mayo Clinic
https://www.mayoclinic.org/diseases-conditions/ataxia/symptoms-causes/syc-20355652
webJan 30, 2024 · EA2 involves longer bouts of ataxia, usually lasting from 30 minutes to six hours. These bouts also are triggered by stress. Dizziness and muscle weakness may occur. People with EA2 may feel very tired. Sometimes symptoms resolve later in life. Episodic ataxia doesn't shorten life span, and symptoms may respond to medicine. Autosomal …
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Spinocerebellar Ataxia - StatPearls - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/NBK557816/
webSep 15, 2023 · Ataxia is the absence of voluntary muscle coordination and loss of control of movement that affects gait stability, eye movement, and speech. Spinocerebellar ataxia (SCA) is an inherited (autosomal dominant), progressive, neurodegenerative, and heterogeneous disease that mainly affects the cerebellum.
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Ataxia - StatPearls - NCBI Bookshelf - National Center for
https://www.ncbi.nlm.nih.gov/books/NBK562284/
webAug 23, 2023 · Ataxia is a neurological sign that manifests in a lack of coordination in the movement of different muscles in the body. It is a clinical finding and not a disease, which mainly presents abnormalities in gait, changes in speech such as scanning speech, and abnormal eye movements such as nystagmus.
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Spinocerebellar ataxia type 2: MedlinePlus Genetics
https://medlineplus.gov/genetics/condition/spinocerebellar-ataxia-type-2/
webSpinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA2 include additional movement problems, speech and swallowing difficulties, and weakness in the muscles ...
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Spinocerebellar Ataxias including Machado-Joseph Disease
https://www.ninds.nih.gov/health-information/disorders/spinocerebellar-ataxias-including-machado-joseph-disease
webNov 28, 2023 · Decreased muscle tone. Vision problems, particularly with focusing the eyes and unwanted eye movements. Difficulty speaking (dysarthria) and swallowing (dysphagia) Cognitive problems (thinking, remembering, and concentration) Most common forms of SCA. The most common forms of SCA are types 1, 2, 3, and 6, which account for most of the …
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Spinocerebellar Ataxia (SCA): Symptoms, Causes & Types - Cleveland Clinic
https://my.clevelandclinic.org/health/diseases/24077-spinocerebellar-ataxia
webSpinocerebellar ataxia (SCA) is a group of inherited brain disorders. It affects your cerebellum, a part of your brain vital to coordination of physical movement, and sometimes your spinal cord. This inherited condition worsens over time and causes specific problems with coordination, usually affecting: Eyes. Hands. Legs and mobility. Speech.
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SCA2 - National Ataxia Foundation
https://www.ataxia.org/sca-2/
webAbout NAF. SCA2. A collection of resources for individuals and families affected by Spinocerebellar Ataxia Type 2 (SCA2). WEBINARS. RESEARCH PIPELINE. INFORMATION. RESEARCH NEWS. BECOME A MEMBER >> SCA2 is caused by a genetic mutation that is passed on from parents to their children.
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Spinocerebellar Ataxia Type 2 (SCA2) - National Ataxia …
https://www.ataxia.org/wp-content/uploads/2019/04/SCA2.pdf
webSpinocerebellar 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 degeneration of the cerebellum (the coordination center of the brain).
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Frontiers | Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects
https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2017.00472/full
webSep 11, 2017 · Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant cerebellar ataxia that occurs as a consequence of abnormal CAG expansions in the ATXN2 gene. Progressive clinical features result from the neurodegeneration of cerebellum and extra-cerebellar structures including the pons, the basal ganglia, and the cerebral cortex.
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