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Results 1 - 10 of 104 for Optic atrophy 9
  1. ... V, Bonneau D, Reynier P, Milea D. Dominant optic atrophy. Orphanet J Rare Dis. 2012 Jul 9;7:46. doi: 10.1186/1750-1172-7- ... D. OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. J Med Genet. 2004 Sep;41(9):e110. doi: 10.1136/jmg.2003.016576. No ...
  2. ... D. OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. J Med Genet. 2004 Sep;41(9):e110. doi: 10.1136/jmg.2003.016576. No ...
  3. ... Patel VR, Sadun AA. Hereditary, nutritional, and toxic optic atrophies. In: Yanoff M, Duker JS, eds. Ophthalmology . 5th ed. Philadelphia, PA: Elsevier; 2019:chap 9.9. Thurtell MJ, Prasad S, Tomsak RL. Neuro-ophthalmology: ...
  4. Macular Degeneration/Treatments and Therapies ... Macular Degeneration ... National Eye Institute ... From the National Institutes of Health ... The Age-Related Eye Disease ...
  5. ... Registry: Arts syndrome Lethal ataxia with deafness and optic atrophy ... and loss of vision in early childhood with a fatal course. Ann Neurol. 1993 May;33(5):535-9. doi: 10.1002/ana.410330519. Citation on PubMed ...
  6. ... aciduria type III Autosomal recessive OPA3 Autosomal recessive optic atrophy 3 Costeff optic atrophy syndrome Infantile optic atrophy with chorea and spastic ...
  7. ... to their children. Hereditary optic neuroretinopathy Leber hereditary optic atrophy Leber optic atrophy Leber's hereditary optic neuropathy Leber's optic ...
  8. ... carry information from the eyes to the brain (optic atrophy), and a number of other features involving the ... that is characterized by progressive hearing loss and optic atrophy leading to vision loss, typically beginning in adolescence. ...
  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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