Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
Synonyms: CAPOS syndrome | Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome
A rare autosomal dominant neurological disorder characterized by early onset cerebellar ataxia associated with areflexia progressive optic atrophy sensorineural deafness a pes cavus deformity and abnormal eye movements.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome?
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Advocacy Organizations
KIF1A.ORG
KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure.
National Ataxia Foundation
To accelerate the development of treatments and a cure while working to improve the lives of those living with Ataxia.
Clinical Trials
For a list of clinical trials in this disease area, please click here.