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1,147 Possible Causes for Progressive Retinitis Pigmentosa

  • Retinitis Pigmentosa

    PURPOSE: To determine whether cataract surgery accelerates disease progression in retinitis pigmentosa (RP). DESIGN: Retrospective cohort study.[ncbi.nlm.nih.gov] KEYWORDS: Disease progression; Ellipsoid zone; Retinitis pigmentosa; SD-OCT; Siblings[ncbi.nlm.nih.gov] Retinitis pigmentosa may be caused by mutations in any one of at least ten different genes, resulting in a malfunction in the retinal pigment epithelial (RPE) cells and a[healthcommunities.com]

  • Usher Syndrome Type 2A

    retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in the USH2A gene on chromosome 1q41.[zfin.org] The affected individuals have sensory-neural deficiencies at birth and subsequently develop progressive retinitis pigmentosa (RP).[abcam.com] retinitis pigmentosa, maps to the long arm of human chromosome 1q41 between markers AFM268ZD1 and AFM144XF2.[science.sciencemag.org]

  • Retinitis

    Retinitis pigmentosa may be caused by mutations in any one of at least ten different genes, resulting in a malfunction in the retinal pigment epithelial (RPE) cells and a[healthcommunities.com] The results are promising, and scientists think that TUNCA holds great potential to treat later-onset and slower progressing retinitis pigmentosa.[retinitispigmentosatreatment.com] General Information Retinitis pigmentosa, or RP, is a group of inherited eye diseases that cause degeneration of the retina and progressive vision loss.[envisionus.com]

  • Usher Syndrome Type 1

    retinitis pigmentosa.[eric.ed.gov] An autosomal recessive condition characterized by sensorineural hearing loss and progressive loss of vision due to retinitis pigmentosa.[medical-dictionary.thefreedictionary.com] USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[uniprot.org]

  • Usher Syndrome Type 1D

    Usher syndrome (USH) is a group of autosomal recessive sensory disorders characterized by progressive retinitis pigmentosa (RP) and sensorineural hearing impairment.[ncbi.nlm.nih.gov] An autosomal recessive condition characterized by sensorineural hearing loss and progressive loss of vision due to retinitis pigmentosa.[medical-dictionary.thefreedictionary.com] USH1 is characterised by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[medical-dictionary.thefreedictionary.com]

  • Usher Syndrome

    retinitis pigmentosa with and without a vestibular abnormality is the… (More)[semanticscholar.org] It has an autosomal recessive pattern of inheritance that results in hearing impairment and progressive retinitis pigmentosa, an eye disorder that causes a person’s vision[ushersyndrome.wordpress.com] The affected individuals have sensory-neural deficiencies at birth and subsequently develop progressive retinitis pigmentosa (RP).[abcam.com]

  • Usher Syndrome Type 1J

    USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness[genecards.org] retinitis pigmentosa (RP).[centogene.com] Onset of retinitis pigmentosa occurs during childhood, resulting in a progressively constricted visual field and impaired visual acuity which rapidly proceeds to blindness[centogene.com]

  • Retinitis pigmentosa 40

    Year 1996 Retinitis pigmentosa (RP) refers to a group of related diseases that tend to run in families and cause slow but progressive loss of vision.[retinaldiagnostic.com] Retinitis Pigmentosa (or RP) is a hereditary disease whereby there is progressive retinal degeneration in both eyes over a period of time.[carolinaeyemd.com] General Information Retinitis pigmentosa, or RP, is a group of inherited eye diseases that cause degeneration of the retina and progressive vision loss.[envisionus.com]

  • Retinitis Pigmentosa 30

    […] of retinitis pigmentosa.[raysahelian.com] Retinitis Pigmentosa involves a progressive loss of visual acuity, defects in the visual field and night blindness.[barcelonamaculafound.org] Journal international d… 2011 DOI: 10.1159/000320500 PURPOSE To assess the effects of nilvadipine on the progression of central visual field defect in retinitis pigmentosa[semanticscholar.org]

  • Metabolic Syndrome

    retinal degeneration or retinitis pigmentosa and neurosensory hearing loss or deafness, cardiomyopathy, and other endocrine disorders.[ncbi.nlm.nih.gov] […] characterized by early-onset severe abdominal obesity, impaired glucose tolerance or type 2 diabetes with insulin resistance, acanthosis nigricans, hyperlipidemia, childhood progressive[ncbi.nlm.nih.gov]

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