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Autosomal recessive cerebellar ataxia

rare

Autosomal recessive cerebellar ataxias (ARCA) are a heterogeneous group of rare neurological disorders involving both the central and peripheral nervous system (and in some cases other systems and organs), and characterized by degeneration or abnormal development of the cerebellum and spinal cord and, in most cases, early onset occurring before the age of 20 years.

Identifiers
MONDO:0015244 Orphanet:1172
Part of
Autosomal recessive diseaseHereditary cerebellar ataxia
Also known as
ARCA · cerebellar ataxia, autosomal recessive

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal recessive congenital cerebellar ataxia 29
Autosomal recessive degenerative and progressive cerebellar ataxia 11
Autosomal recessive metabolic cerebellar ataxia 9
Autosomal recessive syndromic cerebellar ataxia 7
Autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome 3
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3
Charlevoix-Saguenay spastic ataxia
Lichtenstein-Knorr syndrome
RIDDLE syndrome
Ataxia with oculomotor apraxia type 3
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive ataxia, Beauce type
Autosomal recessive spinocerebellar ataxia 10
Autosomal recessive spinocerebellar ataxia 14
Autosomal recessive spinocerebellar ataxia 16
Autosomal recessive spinocerebellar ataxia 20
Autosomal recessive spinocerebellar ataxia 7
Infantile-onset autosomal recessive nonprogressive cerebellar ataxia
Spinocerebellar ataxia, autosomal recessive 22
Spinocerebellar ataxia, autosomal recessive 24
Spinocerebellar ataxia, autosomal recessive 25
Spinocerebellar ataxia, autosomal recessive 26
Spinocerebellar ataxia, autosomal recessive 27
Spinocerebellar ataxia, autosomal recessive 28
Spinocerebellar ataxia, autosomal recessive 29
Spinocerebellar ataxia, autosomal recessive 30
Spinocerebellar ataxia, autosomal recessive 31
Spinocerebellar ataxia, autosomal recessive 32
Spinocerebellar ataxia, autosomal recessive 33

Rare disease

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