spinocerebellar ataxia type 3 | Spinocerebellar ataxia type 3

Keyword	CPC	PCC	Volume	Score	Length of keyword
spinocerebellar ataxia type 3	0.09	0.9	2277	29	29
spinocerebellar	1.69	0.6	2160	36	15
ataxia	0.67	0.8	1174	99	6
type	1.83	0.6	1720	1	4
3	1.13	0.1	5855	7	1

Keyword	CPC	PCC	Volume	Score
spinocerebellar ataxia type 3	1.38	0.5	6472	9
spinocerebellar ataxia type 3 sca3	0.04	0.2	5563	26
spinocerebellar ataxia type 3 symptoms	0.69	0.7	2635	81
spinocerebellar ataxia type 3 treatment	1.33	0.6	2533	6
spinocerebellar ataxia type 3 icd 10	1.96	1	6116	91
spinocerebellar ataxia type 3 prognosis	1.97	0.1	3749	85
spinocerebellar ataxia type 35	0.26	0.6	186	7
spinocerebellar ataxia type 36	1.65	0.4	1537	100
spinocerebellar ataxia type 3 hcc	0.77	0.1	9432	28
what is spinocerebellar ataxia type 3	1.67	0.9	7792	84
icd 10 code for spinocerebellar ataxia type 3	1.24	1	1354	78
spinocerebellar ataxia type 34	0.68	0.1	7556	56

Search Results related to spinocerebellar ataxia type 3 on Search Engine

Spinocerebellar ataxia type 3 - About the Disease - Genetic and …
nih.gov

https://rarediseases.info.nih.gov/diseases/6801/spinocerebellar-ataxia-type-3/

WEBSpinocerebellar ataxia 3 (SCA3) is a rare, inherited form of ataxia. Signs and symptoms may begin between childhood and late adulthood and vary greatly. Symptoms may include slowly progressive clumsiness in the arms and legs; a manner of walking (gait) that may be mistaken for drunkenness; difficulty speaking and swallowing; impaired eye ...

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Spinocerebellar Ataxia Type 3 - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1196/

WEBOct 10, 1998 · Summary. Clinical characteristics. Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is characterized by progressive cerebellar ataxia and variable findings including pyramidal signs, a dystonic-rigid extrapyramidal syndrome, significant peripheral amyotrophy and generalized areflexia, progressive …

DA: 75 PA: 29 MOZ Rank: 67

Spinocerebellar ataxia type 3: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/condition/spinocerebellar-ataxia-type-3/

WEBDescription. Spinocerebellar ataxia type 3 (SCA3) 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 SCA3 include speech difficulties, uncontrolled muscle tensing (dystonia), muscle stiffness ...

DA: 60 PA: 97 MOZ Rank: 98

Spinocerebellar Ataxia (SCA): Symptoms, Causes & Types - Cleveland Clinic
clevelandclinic.org

https://my.clevelandclinic.org/health/diseases/24077-spinocerebellar-ataxia

WEBThe most common type is spinocerebellar ataxia type 3, also known as Machado-Joseph disease. How common is spinocerebellar ataxia? SCA is rare. It affects about 1 to 5 people per 100,000. Advertisement. Symptoms and Causes. What causes spinocerebellar ataxia? An inherited gene mutation causes SCA.

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Spinocerebellar Ataxia - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK557816/

WEBSep 15, 2023 · USA.gov. 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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Spinocerebellar ataxia - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Spinocerebellar_ataxia

WEBThere are three forms of spinocerebellar degeneration: Types 1, 2, 3. Symptoms begin during adulthood.) [citation needed] There are five typical autosomal-recessive disorders in which ataxia is a prominent feature: Friedreich ataxia, ataxia-telangiectasia, ataxia with vitamin E deficiency, ataxia with oculomotor apraxia (AOA), spastic ataxia.

DA: 77 PA: 33 MOZ Rank: 72

Spinocerebellar ataxia: an update - PMC - National Center for
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373366/

WEBOct 3, 2018 · The Spinocerebellar ataxias (SCA) are a subset of hereditary cerebellar ataxias that are autosomal dominantly transmitted. They are progressive neurodegenerative diseases that share the clinical features of ataxia, which arise from the progressive degeneration of the cerebellum but can also affect other connected regions, …

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Spinocerebellar Ataxias including Machado-Joseph Disease
nih.gov

https://www.ninds.nih.gov/health-information/disorders/spinocerebellar-ataxias-including-machado-joseph-disease

WEBNov 28, 2023 · Machado-Joseph disease (SCA3) is one of these disorders. The types and severity of symptoms vary among SCAs, but they are progressive, meaning the symptoms worsen with time. Some forms of SCA may progress slowly over a period of years, while others worsen within months.

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Spinocerebellar ataxia | Nature Reviews Disease Primers
nature.com

https://www.nature.com/articles/s41572-019-0074-3

WEBApr 11, 2019 · The spinocerebellar ataxias (SCAs) are a genetically heterogeneous group of autosomal dominantly inherited progressive disorders, the clinical hallmark of which is loss of balance and...

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SCA3/MJD - National Ataxia Foundation
ataxia.org

https://www.ataxia.org/sca3/

WEBSCA3 (also known as Machado-Joseph Disease) is one of the most common types of Spinocerebellar Ataxias. This webinar covers the causes and symptoms of SCA3/MJD, the typical diagnostic journey for those affected, and what to expect for clinical care. Research and Treatment Development for SCA3. Research & Treatment for SCA3/MJD.

DA: 65 PA: 32 MOZ Rank: 58