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527 Possible Causes for Central Scotoma, Marked Macular Degeneration, Mutation in the TTLL5 Gene

  • Cone Rod Dystrophy Type 15
  • Macular Degeneration

    Macular degeneration is deterioration in the central area of the retina, called the macula, said Dr.[livescience.com] Head Mounted Eye Tracking Aide for Loss of Central Vision (HETALCEV) Participants with bilateral central scotomas will be selected for this study during their routine clinical[centerwatch.com] […] vision (central scotoma) that will get bigger without treatment Symptoms appear and progress more rapidly than with dry AMD.[medicalnewstoday.com]

    Missing: Mutation in the TTLL5 Gene
  • Occult Macular Dystrophy

    Geographic Atrophy A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the central[bioportfolio.com] In both eyes, the abnormalities were observed in static perimetry (relative central scotomas), mfERG (significant reduction of P1 amplitude in the central retinas) and OCT[ncbi.nlm.nih.gov] A wedge-shaped visual field defect in the right eye, corresponding to the enlarged disk cupping, and a relative central scotoma in the left were detected.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Vitreous Degeneration

    The central visual loss that marks macular degeneration can make reading, working with the hands, driving, or recognizing people's faces difficult because the center of the[medical-dictionary.thefreedictionary.com] ., a central scotoma). Peripheral vision is preserved in this disease.[medical-dictionary.thefreedictionary.com]

    Missing: Mutation in the TTLL5 Gene
  • Neuronal Ceroid Lipofuscinosis Type 3

    A “bull's eye” type of macular degeneration appears as an early feature. Degeneration of the peripheral retina becomes more marked with time.[journals.lww.com]

    Missing: Mutation in the TTLL5 Gene
  • Peripheral Cone Dystrophy

    Molecular validation of the candidate variants The novel mutation in the TTLL5 gene (c.182–3_182–1delinsAA) was validated using conventional Sanger sequencing according to[molvis.org] Currently, there are no published guidelines to prognosticate STGD macular degeneration.[retinatoday.com] Goldmann perimetry showed full peripheral visual fields but relative central scotomas within the central 20 .[ncbi.nlm.nih.gov]

  • North Carolina Macular Dystrophy

    Currently, there are no published guidelines to prognosticate STGD macular degeneration.[retinatoday.com] Central scotoma corresponded to retinal lesions in two patients.[ncbi.nlm.nih.gov] CONCLUSIONS: Patients had nearly normal visual acuity even though they presented with deep central scotomas and a shift of the center of fixation away from the fovea.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Central Areolar Choroidal Dystrophy

    […] despite marked choriocapillaris atrophy (Leveille et al., 1982).[docslide.com.br] The visual fields revealed a central scotoma. The disorder was transmitted as an autosomal dominant trait.[ncbi.nlm.nih.gov] Central areolar choroidal dystrophy (CACD) is a rare hereditary disorder leading to a central scotoma in middle-aged patients.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Glaucoma

    Contents: Glaucoma diagnosis -- Introduction to glaucoma diagnosis / Douglas J. Rhee -- Basics of aqueous flow and the optic nerve / Arthur J. Sit and Douglas J. Rhee -- Aqueous flow -- Importance of intraocular pressure -- Brief summary of aqueous physiology and IOP -- Measurement of aqueous humor dynamics --[…][worldcat.org]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene
  • Pernicious Anemia

    Visual field examination by perimetry demonstrates a central or cecocentral scotoma.[ispub.com]

    Missing: Marked Macular Degeneration Mutation in the TTLL5 Gene

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