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Results 11 - 20 of 22 for Optic atrophy 16
  1. Spinocerebellar ataxia type 36 
    ... can contribute to the tongue and limb muscle atrophy in affected individuals.Some people with SCA36 have abnormalities of the eye muscles, which can lead to involuntary eye movements ( ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  2. Mucopolysaccharidosis type VI 
    ... useful biomarkers of mucopolysaccharidosis VI. Pathogenetics. 2009 Jun 16;2(1):4. doi: 10.1186/1755-8417-2-4. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-vi - Genetics
  3. Peroxisomal acyl-CoA oxidase deficiency 
    ... 10.1210/en.2012-1137. Epub 2012 Apr 16. Citation on PubMed or Free article on PubMed ... and brainstem atrophy. J Neurol Neurosurg Psychiatry. 2010 Mar;81(3): ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  4. Hypomyelination and congenital cataract 
    ... a clouding of the lens (cataract) in both eyes.People with this condition ... and wasting (atrophy) in their legs, and many affected people eventually ...
    https://medlineplus.gov/.../hypomyelination-and-congenital-cataract - Genetics
  5. Ataxia-pancytopenia syndrome 
    ... neurological problems associated with a loss of tissue (atrophy) and other ... eye movements (nystagmus). These neurological issues worsen over time, ...
    https://medlineplus.gov/.../condition/ataxia-pancytopenia-syndrome - Genetics
  6. Facioscapulohumeral muscular dystrophy 
    ... j.nmd.2011.09.004. Epub 2011 Dec 16. No abstract available. Citation on PubMed Lemmers RJ, ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  7. Sturge-Weber syndrome 
    ... vessels, causing abnormalities in the brain, skin, and eyes from birth. Sturge-Weber syndrome has three major ... a leptomeningeal angioma, and increased pressure in the eye (glaucoma). These features can vary in severity and ...
    https://medlineplus.gov/genetics/condition/sturge-weber-syndrome - Genetics
  8. Fuchs endothelial dystrophy 
    ... doi: 10.1093/hmg/ddm337. Epub 2007 Nov 16. Citation on PubMed Wright AF, Dhillon B. Major ...
    https://medlineplus.gov/.../condition/fuchs-endothelial-dystrophy - Genetics
  9. Autosomal recessive cerebellar ataxia type 1 
    ... progressive problems with movement due to a loss (atrophy) of nerve cells in the part of the ... doi: 10.1212/WNL.0b013e3182815529. Epub 2013 Jan 16. No abstract available. Erratum In: Neurology. 2013 Mar ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  10. Myotonic dystrophy 
    ... disrupts transcription in myotonic dystrophy. Science. 2004 Jan 16;303(5656):383-7. doi: 10.1126/science. ... with guidelines on management. Neuromuscul Disord. 2006 Jun;16(6):403-13. doi: 10.1016/j.nmd. ...
    https://medlineplus.gov/genetics/condition/myotonic-dystrophy - Genetics
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