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Results 1 - 10 of 12 for Hereditary optic atrophy
  1. Leber hereditary optic neuropathy 
    ... change to their children. Hereditary optic neuroretinopathy Leber hereditary optic atrophy Leber optic atrophy Leber's hereditary optic neuropathy ... s optic neuropathy LHON Genetic Testing Registry: Leber optic atrophy Leber hereditary optic neuropathy National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../leber-hereditary-optic-neuropathy - Genetics
  2. Optic atrophy type 1 
    ... Kjer's optic atrophy Optic atrophy, autosomal dominant Optic atrophy, hereditary, autosomal dominant Optic atrophy, juvenile Optic atrophy, Kjer type Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/optic-atrophy-type-1 - Genetics
  3. Charcot-Marie-Tooth disease 
    ... NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR NEUROPATHY, CONGENITAL ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  4. Autosomal dominant optic atrophy and cataract 
    ... V, Bonneau D, Reynier P, Milea D. Dominant optic atrophy. Orphanet J Rare Dis. 2012 ... Childhood-Onset Hereditary Optic Neuropathy. PLoS One. 2017 Jan 12;12( ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  5. Spastic paraplegia type 2 
    ... intellectual disability; involuntary, rhythmic shaking (tremor); and degeneration ... The prevalence of all hereditary spastic paraplegias combined is estimated to be 2 ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  6. Fatty acid hydroxylase-associated neurodegeneration 
    ... in this gene resulting in intellectual decline and optic nerve atrophy were said to have a disorder called FA2H- ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  7. Familial dysautonomia 
    ... and worsening vision due to the shrinking size (atrophy) of optic nerves, which carry information from the eyes to ...
    https://medlineplus.gov/genetics/condition/familial-dysautonomia - Genetics
  8. Aceruloplasminemia 
    ... light-sensitive tissue at the back of the eye (retina) caused by excess iron. The changes result in small opaque spots and areas of tissue degeneration (atrophy) around the edges of the retina. These abnormalities ...
    https://medlineplus.gov/genetics/condition/aceruloplasminemia - Genetics
  9. Infantile-onset ascending hereditary spastic paralysis 
    ... paraplegia). The spasticity and paraplegia result from degeneration (atrophy) of motor neurons, which are specialized nerve cells in the brain and spinal cord that control muscle movement. Hereditary spastic paraplegias are divided into two types: pure ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics
  10. Hereditary neuralgic amyotrophy 
    ... fold that covers the inner corner of the eye (epicanthal fold), a long nasal bridge, a narrow mouth, and differences between one side of the face and the other (facial asymmetry). Hereditary neuralgic amyotrophy is a rare disorder, but its ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
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