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2,517 Possible Causes for No Retinitis Pigmentosa

  • Retinitis Pigmentosa

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

  • Respiratory Bronchiolitis Interstitial Lung Disease

    In adulthood, many people with retinitis pigmentosa become legally blind. The signs and symptoms of retinitis pigmentosa are most often limited to vision loss.[ghr.nlm.nih.gov] Additional Resources for Retinitis Pigmentosa MedlinePlus: Retinitis Pigmentosa NEI: Retinitis Pigmentosa GARD: Retinitis Pigmentosa Genetics Home Reference: Retinitis Pigmentosa[genome.gov] People with retinitis pigmentosa lose their vision slowly over time. Usually, though, they will not become totally blind. What causes retinitis pigmentosa?[aao.org]

  • IgG4-Related Retroperitoneal Fibrosis

    Additional Resources for Retinitis Pigmentosa MedlinePlus: Retinitis Pigmentosa NEI: Retinitis Pigmentosa GARD: Retinitis Pigmentosa Genetics Home Reference: Retinitis Pigmentosa[genome.gov] People with retinitis pigmentosa lose their vision slowly over time. Usually, though, they will not become totally blind. What causes retinitis pigmentosa?[aao.org] Retinitis pigmentosa (RP) is a term for a group of eye diseases that can lead to loss of sight.[webmd.com]

  • Hallervorden-Spatz Syndrome

    One had retinitis pigmentosa. Neuropsychological testing revealed decreased verbal fluency and visuoconstructional and motor deficits.[ncbi.nlm.nih.gov] Each patient had spastic gait, dysarthria, dystonic posturing of both arms and generalized hyperreflexia, but no Kayser-Fleischer rings or retinitis pigmentosa.[ncbi.nlm.nih.gov] pigmentosa, optic atrophy, oculomotor abnormalities, positive family history and acanthocytosis.[ncbi.nlm.nih.gov]

  • Posterior Subcapsular Cataract

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

  • Retinal Hemorrhage

    In adulthood, many people with retinitis pigmentosa become legally blind. The signs and symptoms of retinitis pigmentosa are most often limited to vision loss.[ghr.nlm.nih.gov] Additional Resources for Retinitis Pigmentosa MedlinePlus: Retinitis Pigmentosa NEI: Retinitis Pigmentosa GARD: Retinitis Pigmentosa Genetics Home Reference: Retinitis Pigmentosa[genome.gov] People with retinitis pigmentosa lose their vision slowly over time. Usually, though, they will not become totally blind. What causes retinitis pigmentosa?[aao.org]

  • Deafness, Autosomal Dominant 23

    pigmentosa syndrome DeafTeen Quest DeafYouth Ministries, Inc DEAG deagglomeration Deagle DEAH DEAH (Asp-Glu-Ala-Asp/His) box polypeptide 57 DEAH (Asp-Glu-Ala-His) box polypeptide[medical-dictionary.thefreedictionary.com] , autosomal dominant 23 22 Retinitis pigmentosa, autosomal recessive 43 41 Retinitis pigmentosa, X-linked 5 2 Syndromic/systemic diseases with retinopathy, autosomal dominant[sph.uth.edu] pigmentosa.[morl.lab.uiowa.edu]

  • Retinopathy

    Download our full guide on retinitis pigmentosa as a PDF (1.3MB) You can also download our full guide on retinitis pigmentosa as a Word document (30KB) Causes of retinitis[rnib.org.uk] What can be done about retinitis pigmentosa? Unfortunately, there is no effective treatment to stop or cure retinitis pigmentosa.[my.clevelandclinic.org] Retinitis pigmentosa (RP) is a term for a group of eye diseases that can lead to loss of sight.[webmd.com]

  • High Myopia-Sensorineural Deafness Syndrome

    Pigmentosa Apparent after first decade of life Electroretinography can identify abnormalities in photoreceptor function in children as young as 2 - 4 Pendred Syndrome Most[en.wikibooks.org] The most common form of cone-rod dystrophy is retinitis pigmentosa .[afb.org] pigmentosa.[medpagetoday.com]

  • Optic Disc Drusen

    The posterior microphthalmos, retinitis pigmentosa and optic disc drusen syndrome was described for the first time in literature in 1991.[ncbi.nlm.nih.gov] Although the associations of retinitis pigmentosa (RP) with nanophthalmos/microphthalmos and RP with optic disc drusen have previously been recognized, the concurrence of[ncbi.nlm.nih.gov] PURPOSE: The purpose of this study is to identify the genetic defect in a Turkish family with autosomal recessive retinitis pigmentosa, nanophthalmos, and optic disc drusen[ncbi.nlm.nih.gov]

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