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165 Possible Causes for Marked Macular Degeneration, Mutation in the TTLL5 Gene, Slit-Lamp Test Abnormal

  • Uveitis

    Morland, Mark W. Greenlee and Frans W. Cornelissen, Morphometric analyses of the visual pathways in macular degeneration, Cortex, 56, (99), (2014).[doi.org]

    Missing: Mutation in the TTLL5 Gene
  • Keratitis

    To report a case of bilateral non-tuberculous mycobacterial keratitis after small incision lenticule extraction (SMILE) that was successfully treated with oral and topical fortified antibiotics. Case report and literature review. An otherwise healthy 21-year-old woman presented with culture-proven bilateral[…][ncbi.nlm.nih.gov]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Cone Rod Dystrophy Type 15
    Missing: Slit-Lamp Test Abnormal
  • Iritis

    Abstract Acute iritis, which is often seen in young adults, may cause red eye, photophobia, and aching discomfort. Many times, the condition can be ameliorated or completely reversed by cautious use of cycloplegic agents and corticosteroids. However, undiagnosed or improperly treated iritis can lead to glaucoma and[…][ncbi.nlm.nih.gov]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Herpes Simplex Dendritic Keratitis

    We treated three patients with herpes simplex dendritic keratitis that occurred between three and 11 months after keratoplasty. The patients had no history of herpetic infection. The eyes of two of the patients were grafted for corneal scarring of undetermined origin. The eye of the third patient was grafted[…][ncbi.nlm.nih.gov]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Interstitial Keratitis

    A slit-lamp examination is essential. Recent work has suggested that high-resolution MRI and antibodies to inner ear antigens may be helpful.[dizziness-and-balance.com] While the ESR, WBC, C-reactive protein test may be abnormal and there may be thrombocytosis or anemia, none of these findings are reliable indicators of the disease.[dizziness-and-balance.com]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Herpes Simplex Keratoconjunctivitis

    الصفحة 100 - MEDAWAR, PB 1948. Immunity to homologous grafted skin. III. The fate of skin homografts transplanted to the brain, to subcutaneous tissue, and to the anterior chamber of the eye. ‏ الصفحة 147 - A. (1996). Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele. Nature 380,[…][books.google.com]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Keratitis Bullosa

    Abstract Histological examination can differentiate between Fuchs' dystrophy of the cornea and the bullous keratopathy which occurs after cataract extraction, with or without the implantation of an artificial lens. The differences are apparent in Descemet's membrane and the endothelium. In 89% of cases there was[…][link.springer.com]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Wilson Disease

    The diagnosis of WD was based on clinical presentation, familial history, Kayser-Fleischer rings detected by slit lamp, low serum ceruloplasmin, abnormally high 24-h urinary[scielo.br] […] copper excretion, liver biopsy, a genetic test and/ or response to a D-penicillamine provocative test.[scielo.br]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Oculomotor Apraxia

    Oculomotor apraxia Other names Cogan ocular motor apraxia or saccadic initiation failure Specialty Ophthalmology Oculomotor apraxia ( OMA ), is the absence or defect of controlled, voluntary, and purposeful eye movement. [1] It was first described in 1952 by the American ophthalmologist David Glendenning Cogan. [2][…][en.wikipedia.org]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene