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Results 31 - 40 of 43 for Retinal degeneration
  1. X-linked juvenile retinoschisis 
    ... affects cells in the central area of the retina called the macula. The macula is ... degeneration, which disrupts the normal functioning of the macula. ...
    https://medlineplus.gov/.../x-linked-juvenile-retinoschisis - Genetics
  2. CFI gene 
    ... has also been associated with age-related macular degeneration (AMD). AMD is a leading cause of vision loss among older adults. It is characterized by damage to the retina and a loss of sharp vision (visual acuity). ...
    https://medlineplus.gov/genetics/gene/cfi - Genetics
  3. Autosomal dominant vitreoretinochoroidopathy 
    ... eye (cataract). In addition, some people have breakdown (degeneration) of the vitreous or the choroid.A characteristic feature of ADVIRC, visible with a special eye exam, is a circular band of excess coloring (hyperpigmentation) in the retina. This feature can help physicians diagnose the disorder. ...
    https://medlineplus.gov/...osomal-dominant-vitreoretinochoroidopathy - Genetics
  4. NGLY1-congenital disorder of deglycosylation 
    ... function. Some affected individuals have eye abnormalities, including degeneration of the nerves that carry information from the eyes to the brain (optic atrophy) and changes in the light-sensing tissue at the back of the eye (the retina). A reduction or absence of tears (hypolacrima or ...
    https://medlineplus.gov/...y1-congenital-disorder-of-deglycosylation - Genetics
  5. Wagner syndrome 
    ... cell is sufficient to cause the disorder. Hyaloideoretinal degeneration of Wagner VCAN-related vitreoretinopathy Wagner disease Wagner vitreoretinal degeneration Wagner vitreoretinopathy Genetic Testing Registry: Wagner syndrome Wagner ...
    https://medlineplus.gov/genetics/condition/wagner-syndrome - Genetics
  6. Bietti crystalline dystrophy 
    ... crystalline corneoretinal dystrophy Bietti crystalline retinopathy Bietti tapetoretinal degeneration with marginal corneal dystrophy Genetic Testing Registry: Bietti ...
    https://medlineplus.gov/.../condition/bietti-crystalline-dystrophy - Genetics
  7. Norrie disease 
    ... Atrophia bulborum hereditaria Congenital progressive oculo-acoustico-cerebral degeneration Episkopi blindness Fetal iritis syndrome Norrie syndrome Norrie' ...
    https://medlineplus.gov/genetics/condition/norrie-disease - Genetics
  8. Saul-Wilson syndrome 
    ... may experience joint pain (osteoarthritis) due to breakdown (degeneration) of ... of the light-sensitive layer (retina) at the back of the eye can cause ...
    https://medlineplus.gov/genetics/condition/saul-wilson-syndrome - Genetics
  9. GUCY2D gene 
    ... major gene responsible for autosomal dominant progressive cone degeneration. Invest ... in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant ...
    https://medlineplus.gov/genetics/gene/gucy2d - Genetics
  10. CLN11 disease 
    ... develop another condition called GRN-related frontotemporal lobar degeneration in which cognitive decline begins between a person' ... functional progranulin protein develop GRN-related frontotemporal lobar degeneration. Ceroid lipofuscinosis, neuronal, 11 GRN-related neuronal ceroid- ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
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