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posterior column ataxia-retinitis pigmentosa syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Posterior column ataxia - retinitis pigmentosa is characterized by the association of progressive sensory ataxia and retinitis pigmentosa.
Uniprot Description A neurodegenerative syndrome beginning in infancy with areflexia and retinitis pigmentosa. Nyctalopia (night blindness) and peripheral visual field loss are usually evident during late childhood or teenage years, with subsequent progressive constriction of the visual fields and loss of central retinal function over time. A sensory ataxia caused by degeneration of the posterior columns of the spinal cord results in a loss of proprioceptive sensation that is clinically evident in the second decade of life and gradually progresses. Scoliosis, camptodactyly, achalasia, gastrointestinal dysmotility, and a sensory peripheral neuropathy are variable features of the disease. Affected individuals have no clinical or radiological evidence of cerebral or cerebellar involvement.
Mondo Term and Equivalent IDs
MONDO:0012177:  posterior column ataxia-retinitis pigmentosa syndrome
GARD:0009898: 
MESH:C536343: 
Orphanet:88628: 
SCTID:724065003: 
UMLS:C1836916: 
UMLS:C4510304: