Autosomal dominant optic atrophy and cataract is an eye disorder that is characterized by impaired vision. Most affected individuals have decreased sharpness of ...

Optic atrophy type 1 is a condition that often causes slowly worsening vision, usually beginning in childhood. People with optic atrophy type 1 typically experience a narrowing of their ...

... aciduria type III Autosomal recessive OPA3 Autosomal recessive optic atrophy 3 Costeff optic atrophy syndrome Infantile optic atrophy with chorea and spastic ...

... to their children. Hereditary optic neuroretinopathy Leber hereditary optic atrophy Leber optic atrophy Leber's hereditary optic neuropathy Leber's optic ...

... the eyes to the brain (a condition called optic atrophy). People with Wolfram syndrome often also have pituitary ... who develops diabetes mellitus requires insulin replacement therapy. Optic atrophy is often the next symptom to appear, usually ...

... gene have been found to cause autosomal dominant optic atrophy and cataract. This condition causes slowly worsening vision ... in the OPA3 gene that cause autosomal dominant optic atrophy and cataract occur in one copy of the ...

... carry information from the eyes to the brain (optic atrophy).It is unclear how MFN2 gene mutations lead ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A MITOFUSIN 2; MFN2 NCBI Gene ClinVar Ando ...

... with deafness and loss of vision Ataxia-deafness-optic atrophy, lethal Genetic Testing Registry: Arts syndrome Lethal ataxia with deafness and optic atrophy National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...

... carry information from the eyes to the brain (optic atrophy). Affected individuals can develop an increased sensitivity to ... blindness, dystonia, fractures, and mental deficiency Deafness-dystonia-optic atrophy syndrome Jensen syndrome Mohr-Tranebjærg syndrome Opticoacoustic nerve ...