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2,470 Possible Causes for Retinitis Pigmentosa

  • Congenital Deafness

    LXXIX The Association of Nerve Deafness and Retinitis Pigmentosa Interval Report . Annals of Otology, Rhinology & Laryngology, Vol. 69, Issue. 4, p. 1044.[] Some families with atypical late onset retinitis pigmentosa and borderline vestibular dysfunction.[] Both Usher syndrome types 1 and 2 are recessive disorders which cause congenital hearing loss and late-onset blindness due to retinitis pigmentosa.[]

  • Retinitis Pigmentosa

    What is Retinitis Pigmentosa? Retinitis Pigmentosa is the name given to a hereditary disease of the retina in the eye.[] Heredity is the major factor for development of retinitis pigmentosa.[] Gamm Retinitis pigmentosa Additional Information[]

  • Optic Neuropathy

    Retinal degeneration (eg, retinitis pigmentosa ). Retinal storage diseases (eg, Tay-Sachs disease ). Radiation neuropathy. Syphilis.[] Consecutive optic atrophy In consecutive optic atrophy (eg, retinitis pigmentosa, myopia, central retinal artery occlusion), the disc is waxy pale with a normal disc margin[]

  • Neuronal Ceroid Lipofuscinosis

    Weleber, Retinitis Pigmentosa and Allied Disorders, Retina, 10.1016/B978-1-4557-0737-9.00040-0, (761-835), (2013).[] Neuro-ophthalmological abnormalities like optic atrophy (50%), macular degeneration (33.3%) and retinitis pigmentosa (8.3%) were seen in two thirds.[] Weleber, Retinitis Pigmentosa and Allied Disorders, Retina, 10.1016/B978-1-4557-0737-9.00040-0, (761-835), (2013). María S.[]

  • Hereditary Motor and Sensory Neuropathy

    The association between HMSN and retinitis pigmentosa or optic atrophy is sometimes described.[] HMSN7 HMSN retinitis pigmentosa 32094 — Later onset with muscular weakness and atrophy mostly in the lower extremities.[] HMSN VII refers to HMSN associated with an inherited optic atrophy ( OPTIC ATROPHIES, HEREDITARY ), and HMSN VII refers to HMSN associated with retinitis pigmentosa.[]

  • Syphilis

    There is no proven alternative to penicillin for treatment of maternal syphilis. We report 2 case-patients with maternal syphilis who were successfully treated without penicillin. We used amoxicillin and probenecid for the first case-patient and amoxicillin, probenecid, and ceftriaxone for the second case-patient.[]

  • Laurence Moon Syndrome

    Moon: Four cases of «retinitis pigmentosa» occurring in the same family, and accompanied by general imperfections of development.[] From Wikidata Jump to navigation Jump to search rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities[] Synonyms: adipogenital-retinitis pigmentosa syndrome, LM syndrome This is a rare autosomal recessive condition.[]

  • Usher Syndrome

    PURPOSE: The purpose of this study was to examine cone photoreceptor structure in retinitis pigmentosa (RP) and Usher syndrome using confocal and nonconfocal split-detector[] Here we describe a syndrome in five brothers with the distinctive presentation of late-onset progressive hearing loss, cataracts, retinitis pigmentosa, sperm motility and[] PURPOSE: Retinitis pigmentosa (RP), a major cause of blindness in developed countries, has multiple causative genes; its prevalence differs by ethnicity.[]

  • Usher Syndrome Type 1

    In view of the combination of profound hearing loss, vestibular dysfunction, and retinitis pigmentosa in the patients, we classified the disease as USH1.[] Abstract Usher syndrome is an autosomal recessive disease associating congenital sensorineural deafness and retinitis pigmentosa.[] Abstract Usher syndrome (USH) is a clinically and genetically heterogeneous disorder characterized by congenital hearing loss combined with retinitis pigmentosa.[]

  • Posterior Subcapsular Cataract

    Purpose: Posterior subcapsular cataract (PSC) is a frequent complication in patients with retinitis pigmentosa (RP).[] retinitis pigmentosa (rod-cone degeneration), cone-rod degeneration, Usher's syndrome, and choroideremia.[] It is reported to happen rapidly in individuals on steroids, or amongst patients with diabetes, high-grade myopia or retinitis pigmentosa.[]

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