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493 Possible Causes for Mutation in the TTLL5 Gene, Progressive Loss of Visual Acuity

  • Common Cold

    Visual acuity loss was not significantly affected by zinc supplementation alone.[ods.od.nih.gov] A follow-up AREDS2 study confirmed the value of this supplement in reducing the progression of AMD over a median follow-up period of 5 years [ 78 ].[ods.od.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Goldmann-Favre Syndrome

    A 21-year-old woman complained of progressive loss of visual acuity. She had also had night blindness since she was ten years old.[ncbi.nlm.nih.gov] GFS manifests with progressive loss of visual acuity and night blindness. Peripheral vision can be decreased. Cataract is a frequent complication.[orpha.net] Prognosis GFS has a progressive course. In most cases, visual loss occurs in the first two decades of life.[orpha.net]

    Missing: Mutation in the TTLL5 Gene
  • Cone Rod Dystrophy Type 15
  • Autosomal Dominant Optic Atrophy

    Abstract Autosomal dominant optic atrophy (ADOA) is the most prevalent hereditary optic neuropathy resulting in progressive loss of visual acuity, centrocoecal scotoma and[ncbi.nlm.nih.gov] This disorder presents in childhood with progressive loss of visual acuity that is usually bilateral, centrocecal scotoma that is typically symmetrical, and bilateral temporal[athenadiagnostics.com] The affected family members exhibited early-onset and progressive visual impairment, resulting in mild to profound loss of visual acuity.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Optic Atrophy

    This disorder presents in childhood with progressive loss of visual acuity that is usually bilateral, centrocecal scotoma that is typically symmetrical, and bilateral temporal[athenadiagnostics.com] Clinical features of ADOA include a slowly progressive bilateral loss of visual acuity, constriction of peripheral visual fields, central scotomas, and color vision abnormalities[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Thrombosis

    Visual loss is often insidious, with progressive constriction of the visual fields and relative sparing of central visual acuity.[stroke.ahajournals.org] Visual Loss Severe visual loss due to CVT rarely occurs (2% to 4%). 55, 193, 235 Papilledema can cause transient visual impairment, and if prolonged, optic atrophy and blindness[stroke.ahajournals.org]

    Missing: Mutation in the TTLL5 Gene
  • Keratitis

    The patient presented with progressive loss of vision with best-corrected visual acuity 20/40. Immature cataract with 1.43D against the rule astigmatism was noted.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Acute Zonal Occult Outer Retinopathy

    acuity and 21 systemic corticosteroid-treated eyes with progressive visual acuity loss.[ncbi.nlm.nih.gov] […] with progressive visual acuity loss.[ncbi.nlm.nih.gov] Over her 13-year follow-up, best-corrected visual acuity dropped to 20/60 in both eyes and visual field loss because of chorioretinal atrophy progressed significantly.[ncbi.nlm.nih.gov]

    Missing: Mutation in the TTLL5 Gene
  • Cerebral Thrombosis

    Visual loss is often insidious, with progressive constriction of the visual fields and relative sparing of central visual acuity.[ahajournals.org] Visual Loss Severe visual loss due to CVT rarely occurs (2% to 4%). 55 , 193 , 235 Papilledema can cause transient visual impairment, and if prolonged, optic atrophy and blindness[ahajournals.org]

    Missing: Mutation in the TTLL5 Gene
  • Wolfram Syndrome

    She began to complain of progressive loss of visual acuity at the age of 16 and four years later bilateral atrophy of the optic nerves was detected.[jmg.bmj.com] Patients present a progressive reduction of visual acuity and loss of color vision (leading to vision of 6/60 or less in the better eye over an average of 8 years).[orpha.net] Ophthalmological examination showed a progressive loss of visual acuity owing to bilateral optic atrophy (0.6 and 0.8 at the age of 7, 0.1, and 0.3 at the age of 13 for the[jmg.bmj.com]

    Missing: Mutation in the TTLL5 Gene

Further symptoms