dbo:abstract
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- CAPOS syndrome is a rare genetic neurological disorder which is characterized by abnormalities of the feet, eyes and brain which affect their normal function. These symptoms occur episodically when a fever-related infection is present within the body. (en)
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dbo:alias
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- (en)
- CAPOS (en)
- CAPOS syndrome. Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome. Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss. (en)
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dbo:wikiPageID
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dbo:wikiPageLength
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- 7154 (xsd:nonNegativeInteger)
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dbp:causes
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dbp:complications
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- Blindness, deafness, problems with coordination. (en)
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dbp:deaths
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dbp:duration
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dbp:frequency
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- rare, only 14 cases have been described in medical literature (en)
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dbp:name
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dbp:onset
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dbp:prevention
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dbp:prognosis
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dbp:specialty
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dbp:symptoms
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- Mainly cerebellar ataxia, sensorineural hearing loss, and optic nerve atrophy (en)
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dbp:synonyms
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- CAPOS
CAPOS syndrome. Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome. Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss. (en)
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dbp:treatment
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dbp:types
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- It is a type of ATP1A3-related disorder (en)
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dbp:wikiPageUsesTemplate
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dct:subject
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rdf:type
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rdfs:comment
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- CAPOS syndrome is a rare genetic neurological disorder which is characterized by abnormalities of the feet, eyes and brain which affect their normal function. These symptoms occur episodically when a fever-related infection is present within the body. (en)
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