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2,302 Possible Causes for No Retinal Degeneration

  • Retinitis Pigmentosa

    degeneration (AMD), according to a new report.[] […] the retina leading to progressive sight loss RP pericentral pigmentary retinopathy pigmentary degeneration of the retina edit English retinitis pigmentosa retinal degeneration[] degeneration: six patients with RP and four with the "dry" form of AMD.[]

  • Autosomal Recessive Isolated Optic Atrophy

    Degeneration of retinal ganglion cells and their axons; bilateral subacute optic neuropathy, typically with simultaneous or rapidly sequential central or cecocentral visual[] Optic nerve degeneration and optic atrophy are present in many disorders in which mitochondrial impairment is the underlying cause for the degeneration of retinal cells.[] Genes in the Optic Atrophy Panel and their clinical significance Gene Associated phenotypes Inheritance ClinVar HGMD ACO2 Optic atrophy, Infantile cerebellar-retinal degeneration[]

  • Macular Degeneration

    The Argus II has already been tested and approved in the United States and Europe for individuals with Retinitis Pigmentosa (RP) and Outer Retinal Degeneration, respectively[] Current screening protocols have limitations in detecting the early signs of retinal degeneration.[] Like other macular degenerations, pathogenesis within the retinal pigment epithelium (RPE) appears to contribute to the loss of photoreceptors from the central retina.[]

  • Myopic Macular Degeneration

    The higher grades of staphylomas were associated with more severe myopic retinal degeneration.[] Posted 3 years ago , 3 users are following. hello, i am a 23 year old male and i have been told that I have myopic macular degeneration and have had retinal hemprrhages multiple[] This stretching of the sclera is thought to lead to retinal degeneration.[]

  • Retinal Detachment

    LESSONS: In this case, the retinal degeneration was morphologically different from retinal lattice degeneration, thus suggesting that it might be involved in the onset of[] Asymptomatic retinal breaks and lattice degeneration are visible lesions that are risk factors for later retinal detachment.[] […] hole associated with lattice degeneration, or retinal break that occurs later at a site of lattice degeneration.[]

  • Hallervorden-Spatz Syndrome

    The Hallervorden-Spatz syndrome (HSS) is a rare condition characterized by extrapyramidal and pyramidal signs, dystonia, dysarthria, retinal degeneration, dementia and a progressive[] degeneration and brain iron accumulation.[] PURPOSE: The onset of pantothenate kinase-associated neurodegeneration (PKAN) occurs in the first and second decade of life and a pigmentary retinal degeneration is a feature[]

  • Bonnemann-Meinecke-Reich Syndrome

    Peripheral Retinal Degeneration Information on Peripheral Retinal Degeneration Peripheral Retinal Degeneration is a very common disease.[] Bonnemann-Meinecke-Reich syndrome (BMRS), also known as encephalopathy intracranial calcification growth hormone deficiency microcephaly retinal degeneration, is a rare congenital[] Retinal Degeneration 53 Encephalopathy-Intracerebral Calcification-Retinal Degeneration Syndrome 59 Bonnemann Meinecke Reich Syndrome 53 Bonnemann-Meinecke-Reich Syndrome[]

  • Retinitis

    PURPOSE: Increasing evidence suggests that nerve growth factor (NGF) exerts protective effects against retinal degeneration in animal models of retinitis pigmentosa (RP).[] Most forms of retinitis pigmentosa and related retinal degenerations affect only the eye, although in a minority of cases the retinal degeneration is one feature of a syndrome[] RESULTS: RCS rats showed a significant retinal degeneration associated with cell apoptosis at 40 pd when compared to wild-type animals.[]

  • Lattice Degeneration of the Retina

    Abstract Lattice retinal degeneration is considered the most significant peripheral retinal disorder potentially predisposing to retinal breaks and retinal detachment.[] Non-Billable/Non-Specific Code Type 1 Excludes hereditary retinal degeneration (dystrophy) ( H35.5- ) peripheral retinal degeneration with retinal break ( H33.3- ) Peripheral[] […] areas. retinal tears lattice degenerations retinal detachment Statistics from retinal tears lattice degenerations retinal detachment Many studies of posterior[]

  • Goldmann-Favre Syndrome

    degeneration (CPRD).[] (p. 437) NR2E3-Linked Retinal Degenerations: Enhanced S-Cone Sensitivity Syndrome, Goldmann-Favre Syndrome, Clumped Pigmentary Retinal Degeneration, and Retinitis Pigmentosa[] OBJECTIVES: To determine if enhanced s-cone syndrome (ESCS), Goldmann-Favre syndrome (GFS), and clumped pigmentary retinal degeneration (CPRD) are caused by mutations in the[]

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