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PedAM

Pediatric Disease Annotations & Medicines




Disease cataract
Phenotype C0004134|ataxia
Sentences 2
PubMedID- 22797356 Opa3--related autosomal dominant optic atrophy and cataract with ataxia and areflexia.
PubMedID- 26068213 Although our criteria were mainly the presence of ataxia and polyneuropathy associated with either cataract, a decline in visual acuity and/or hearing loss, it could not exclude the presence of atypical clinical presentations, as was the case for non-algerian pharc patients.

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