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17 Possible Causes for Retinitis Pigmentosa Sector Type

  • Peripheral Vasoproliferative Retinopathy

    Photodynamic treatment of a secondary vasoproliferative tumor associated with sector retinitis pigmentosa and Usher syndrome type I.[retinalphysician.com] Photodynamic treatment of a secondary vasoproliferative tumour associated with sector retinitis pigmentosa and Usher syndrome type I .[nature.com] Retinitis pigmentosa and Coats' disease. Arch Ophthalmol. 1968;79:146-149. 28. Osman SA, Aylin Y, Arikan G, Celikel H.[retinalphysician.com]

  • Retinitis Pigmentosa

    Identification and classification of all retinitis pigmentosa (RP) causing mutations contribute to a better understanding of disease variants.[ncbi.nlm.nih.gov] None of the trials included participants with atypical forms of RP (e.g. paravenous retinitis pigmentosa, clumped pigmentary retinal degeneration, sector retinitis pigmentosa[doi.org] In this report we describe a New Zealand family, of European heritage, affected by a sectoral type RP phenotype in association with a novel rhodopsin mutation (proline-170[ncbi.nlm.nih.gov]

  • Retinal Angioma

    Photodynamic treatment of a secondary vasoproliferative tumor associated with sector retinitis pigmentosa and Usher type I. Clin Exp Ophthalmo1 2007;35:191-3. 11.[meajo.org]

  • Choroid Hemangioma

    Osman SA, Aylin Y, Gul A, Celikel H (2007) Photodynamic treatment of a secondary vasoproliferative tumour associated with sector retinitis pigmentosa and Usher syndrome type[omicsonline.org]

  • Usher Syndrome Type 1C
  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Guanylate cyclase : Leber congenital amaurosis type 1 (LCA1); MIN:204000. H( )-transporting two-sector ATPase : Neuropathy, ataxia, and retinitis pigmentosa; MIN:551500.[changbioscience.com]

  • Usher Syndrome Type 1

    Abstract Usher syndrome (USH) is an autosomal recessive hereditary disorder characterised by congenital sensorineural hearing loss and gradual visual impairment secondary to retinitis pigmentosa (RP). The disorder is clinically and genetically heterogeneous. With regard to Usher type I (USH1), several subtypes have[…][ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1D

    Photodynamic treatment of a secondary vasoproliferative tumour associated with sector retinitis pigmentosa and Usher syndrome type I.[healio.com] Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing loss.[healio.com]

  • Retinal Pigmentary Dystrophy

    In contrast to classical retinitis pigmentosa types, sector retinitis pigmentosa is considered stationary or only very slowly progressive, and the fovea preserves its normal[intechopen.com] Sector retinitis pigmentosa is mostly bilateral, and symmmetric.[intechopen.com]

  • Retinitis Pigmentosa 9

    […] with myopathy, Recessive Newfoundland rod-cone dystrophy, Retinitis pigmentosa sinpigmento, Sector retinitis pigmentosa, Regional retinitis pigmentosa, Senior-Loken syndrome[google.com] , Joubert syndrome, Stargardt disease, juvenile, Stargardt disease, late onset, Dominant macular dystrophy, Stargardt type, Dominant Stargardt-like macular dystrophy, Recessive[google.com] Recessive Refsum disease, adult form, Recessive Refsum disease, infantile form, Recessive enhanced S-cone syndrome, Retinitis pigmentosa with mental retardation, Retinitis pigmentosa[google.com]

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