Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
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Sign InDescription
Syndromic optic atrophy, also known as DOA+ syndrome, is a neurologic disorder characterized most commonly by an insidious onset of visual loss and sensorineural hearing loss in childhood with variable presentation of other clinical manifestations including progressive external ophthalmoplegia (PEO), muscle cramps, hyperreflexia, and ataxia. There appears to be a wide range of intermediate phenotypes (Yu-Wai-Man et al., 2010).
Mode of Inheritance
- Autosomal dominant inheritance
VARIANTS
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