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Results 1 - 10 of 58 for Optic atrophy 3
  1. ... aciduria type III Autosomal recessive OPA3 Autosomal recessive optic atrophy 3 Costeff optic atrophy syndrome Infantile optic atrophy with chorea and ...
  2. ... atrophy, cataract, and neurologic disorder Genetic Testing Registry: Optic atrophy 3 Autosomal dominant optic atrophy and cataract National Organization ...
  3. ... speech (dysarthria), difficulty coordinating movements (ataxia), stiffness (spasticity), optic atrophy, and a decline in intellectual function (dementia).Affected individuals who show symptoms of 3-methylglutaconyl-CoA hydratase deficiency in childhood often go ...
  4. ... visual information from the eyes to the brain (optic nerve atrophy), which can lead to vision loss.DCMA syndrome is associated with increased levels of a substance called 3-methylglutaconic acid in the urine. The amount of ...
  5. ... and worsening vision due to the shrinking size (atrophy) of optic nerves, which carry ... affects about 1 in 3,700 individuals in Ashkenazi Jewish populations. Familial dysautonomia ...
  6. ... to their children. Hereditary optic neuroretinopathy Leber hereditary optic atrophy Leber optic atrophy Leber's hereditary optic neuropathy Leber's optic ...
  7. ... 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 ...
  8. ... 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 ...
  9. ... visual information from the eyes to the brain (optic atrophy). The eye problems impair vision in affected individuals. ... cataracts, microphthalmia, and small pupils. They have milder optic atrophy and cortical visual impairment than people with Warburg ...
  10. ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY; HMSN6B CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; ...
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