BabelNet

bn:16604316n

Noun Concept

No term available

Spinocerebellar ataxia type 6 is a rare, late-onset, autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, oculomotor disorders, peripheral neuropathy, and ataxia of the gait, stance, and limbs due to cerebellar dysfunction. Wikipedia

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Sources

IS A

malattia rara

atassia spinocerebellare

GENETIC ASSOCIATION

CACNA1A

HEALTH SPECIALTY

neurologia