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SCA6

Spinocerebellar ataxia type 6

Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria

Spinocerebellar ataxia

GeneTests Spinocerebellar Ataxias including Machado-Joseph Disease at NINDS sca6 at NIH/UW GeneTests sca7 at NIH/UW GeneTests sca8 at NIH/UW GeneTests Mosemiller

Trinucleotide repeat disorder

(Spinocerebellar ataxia Type 3 or Machado-Joseph disease) ATXN3 12 - 40 55 - 86 SCA6 (Spinocerebellar ataxia Type 6) CACNA1A 4 - 18 21 - 30 SCA7 (Spinocerebellar

Hemiplegic migraine

ataxia. This is unsurprising as subtypes of these disorders (FHM1, EA2 and SCA6) are allelic, i.e., they result from mutations in the same gene. The other

Cav2.1

DW, Amos C, et al. (January 1997). "Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent

Inferior olivary nucleus

cerebellum. These disorders include supranuclear palsy, Leigh disease, and SCA6, and there are several more. These disorders all involve motor coordination

Repeated sequence (DNA)

underlie several types of spinocerebellar ataxias (SCAs-SCA1; SCA2; SCA3; SCA6; SCA7; SCA12; SCA17). Similar to Huntington's disease, the polyglutamine

Q-type calcium channel

(FHM1), episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6). Indelicato E, Unterberger I, Nachbauer W, Eigentler A, Amprosi M, Zeiner

P-type calcium channel

alpha 1A subunit Identifiers Symbol CACNA1A Alt. symbols Cav2.1, CACNL1A4, SCA6, MHP1, MHP IUPHAR 532 NCBI gene 773 HGNC 1388 OMIM 601011 RefSeq NM_000068

Spinocerebellar ataxia type 1

nystagmus following horizontal head shaking reduces the likelihood of an SCA6 diagnosis, while the absence of a square wave pattern during fixation reduces