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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease cone rod dystrophy
Comorbidity C0004134|ataxia
Sentences 7
PubMedID- 24628582 Posterior column ataxia with retinitis pigmentosa (pcarp) is an autosomal recessive disorder characterized by severe sensory ataxia, muscle weakness and atrophy, and progressive pigmentary retinopathy.
PubMedID- 24753676 Bassen and kornzweig first reported the association of ataxia with atypical retinitis pigmentosa (rp) and acanthocytosis in 1950.
PubMedID- 23182644 The mtdna t8993c mutation, associated with narp (neuropathy, ataxia, retinitis pigmentosa) and with maternally-inherited leigh syndrome, was more common in the group without than with exercise intolerance, but the difference did not reach statistical significance.
PubMedID- 21267618 Posterior column ataxia with retinitis pigmentosa in a japanese family with a novel mutation in flvcr1.
PubMedID- 23475516 In this review, we outline some of our recent efforts in the medical genome center at the university of tokyo hospital, including an identification of the causative gene for a mendelian disease (posterior column ataxia with retinitis pigmentosa), an approach to uncover susceptible genes for a non-mendelian disease (parkinson disease), and an application of exome sequencing for the molecular diagnosis of a disease with vast genetic heterogeneity (hereditary diffuse leukoencephalopathy with spheroids).
PubMedID- 22277444 We performed target capture and next-generation sequencing analyses of a small consanguineous family in which only two members were affected by posterior column ataxia with retinitis pigmentosa (pcarp).
PubMedID- 21314015 The best example is the narp (neuropathy, ataxia, retinitis pigmentosa)syndrome, first described by anita harding in 1990 infour maternally related relatives: three adults with sensoryneuropathy, ataxia, exercise intolerance, retinitispigmentosa, and dementia; and one child with developmentaldelay, ataxia, retinitis pigmentosa, and abnormaleeg (5).

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