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100 Possible Causes for Retinal Degeneration Not in All Cases

  • Macular Degeneration

    […] cells - from the retinal pigment epithelium lead to cases of neovascularization, a finding which could be closely related to similar processes in age-related macular degeneration[news-medical.net] […] team of the Medicine Faculty at Valencia Catholic University, headed by Jorge Bacia, have discovered that exosomes - microscopic extracellular vesicles that are released by all[news-medical.net]

  • Retinitis Pigmentosa

    Choroidal dystrophies In all cases there is a marked atrophy of the choriocapillaris that is readily diagnosed by the absence of fluorescence in fluorescein angiography. •[ojrd.com] RP is often associated with other ocular abnormalities in addition to retinal degeneration, such as cataract (clouding of the lens of the eye) or cystoid macular edema (swelling[doi.org] […] of the retinal pigment epithelium with characteristic bear-like footprints in fundus.[ojrd.com]

  • Optic Papillitis

    Regional hypoperfusion should not be secondary to axonal degeneration since all the recruited cases were free from previous optic nerve and retinal disorders.[journals.plos.org]

  • Vitreous Hemorrhage

    These conditions account for 60-89% of all hemorrhage cases. Other less common causes include sickle cell retinopathy and age related macular degeneration.[laretinasurgeon.com] Common conditions include diabetic retinopathy, hypertensive retinal vascular disease, or posterior vitreous detachment.[laretinasurgeon.com]

  • Optic Neuritis

    Regional hypoperfusion should not be secondary to axonal degeneration since all the recruited cases were free from previous optic nerve and retinal disorders.[journals.plos.org]

  • Optic Neuropathy

    It is characterised by bilateral subacute loss of central vision owing to focal degeneration of the retinal ganglion cell layer and optic nerve.[jmg.bmj.com] Over 95% of LHON cases are primarily the result of one of three mitochondrial DNA (mtDNA) point mutations, G3460A, G11778A, and T14484C, which all involve genes encoding complex[jmg.bmj.com]

  • Neuronal Ceroid Lipofuscinosis

    Disease course was severe; all patients were in a vegetative state by the second decade of life, and eventually die prematurely (except in one case).[ncbi.nlm.nih.gov] degeneration.[ncbi.nlm.nih.gov] […] patients of a consanguineous family who presented in early childhood with intractable seizures, severe cognitive and motor decline, behavioral impairment and progressive retinal[ncbi.nlm.nih.gov]

  • Meckel Syndrome Type 7

    cases.[en.wikipedia.org] degeneration. [5] The MKS1 gene has been identified as being associated with a ciliopathy. [6] Diagnosis [ edit ] Dysplastic kidneys are prevalent in over 95% of all identified[en.wikipedia.org] […] known ciliopathies include primary ciliary dyskinesia, Bardet–Biedl syndrome, polycystic kidney and liver disease, nephronophthisis, Alström syndrome, and some forms of retinal[en.wikipedia.org]

  • Exudative Vitreoretinopathy Type 2

    Vitreoretinal adhesion was present in the peripheral temporal retina in all cases.[ncbi.nlm.nih.gov] A V-shaped retinal degeneration was seen along the temporal meridian in 18 cases (48%).[ncbi.nlm.nih.gov]

  • Hereditary Optic Atrophy

    It is characterised by bilateral subacute loss of central vision owing to focal degeneration of the retinal ganglion cell layer and optic nerve.[jmg.bmj.com] Over 95% of LHON cases are primarily the result of one of three mitochondrial DNA (mtDNA) point mutations, G3460A, G11778A, and T14484C, which all involve genes encoding complex[jmg.bmj.com]

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