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Up to: Autosomal recessive disease · Hereditary cerebellar ataxia
Autosomal recessive cerebellar ataxia
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.
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Autosomal recessive degenerative and progressive cerebellar ataxia 0 trials · 49 incl. sub-types Sub-types →
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Autosomal recessive metabolic cerebellar ataxia 0 trials · 10 incl. sub-types Sub-types →
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Autosomal recessive congenital cerebellar ataxia 0 trials · 7 incl. sub-types Sub-types →
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Autosomal recessive syndromic cerebellar ataxia 0 trials · 2 incl. sub-types Sub-types →
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Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 0 trials · 2 incl. sub-types Sub-types →
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Lichtenstein-Knorr syndrome 0 trials
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RIDDLE syndrome 0 trials