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Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment

Retinitis Pigmentosa (RP) is an inherited retinal dystrophy (IRD) that causes progressive visual loss. Patients suffering from RP have a substantial influence on their everyday activities, social contacts, and jobs, lowering their quality of life. Frequent referral delays, as well as the lack of a s...

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Autores principales: Kamde, Saakshi P, Anjankar, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686897/
https://www.ncbi.nlm.nih.gov/pubmed/38034182
http://dx.doi.org/10.7759/cureus.48006
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author Kamde, Saakshi P
Anjankar, Anil
author_facet Kamde, Saakshi P
Anjankar, Anil
author_sort Kamde, Saakshi P
collection PubMed
description Retinitis Pigmentosa (RP) is an inherited retinal dystrophy (IRD) that causes progressive visual loss. Patients suffering from RP have a substantial influence on their everyday activities, social contacts, and jobs, lowering their quality of life. Frequent referral delays, as well as the lack of a standard therapy for the majority of patients, contribute to the significant unmet demand for RP. Any retinal injury has the potential to result in total blindness and visual impairment. Despite the fact that there is no cure for RP, people can manage it using rehabilitation programs and low-vision gadgets. The purpose of this research is to characterize the expanding treatment landscape for RP, as well as the justification for advanced therapy medicinal products (ATMPs). Vitamin A supplements can help prevent the sluggish visual loss caused by a prevalent kind of RP. The presence of visual purple in the rods and the underlying vascular choroid causes the retina to look purplish red. The major portion of the retina damaged is the rod photoreceptor electric cell; the development of diverse diseases is progressive. Because of the retina's accessibility, immunological privilege, and compartmentalization, hereditary retinal diseases are amenable to cell and gene therapy. Therapeutic techniques that attempt to rescue photoreceptors (gene therapies) require the existence of non-functional target cells, but other therapies (cell therapies) do not require the presence of live photoreceptors. To provide successful therapy choices for RP patients at all disease phases, the development pipeline must be continually diversified and advanced, as well as ongoing efforts to encourage early patient identification and quick diagnosis. Future research will focus on avoiding vision loss in genetic eye illnesses and assisting patients in regaining their eyesight. Retinal implants, cell therapies, supplementary medications, and gene therapies may become common treatments for reducing vision loss in the future.
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spelling pubmed-106868972023-11-30 Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment Kamde, Saakshi P Anjankar, Anil Cureus Pathology Retinitis Pigmentosa (RP) is an inherited retinal dystrophy (IRD) that causes progressive visual loss. Patients suffering from RP have a substantial influence on their everyday activities, social contacts, and jobs, lowering their quality of life. Frequent referral delays, as well as the lack of a standard therapy for the majority of patients, contribute to the significant unmet demand for RP. Any retinal injury has the potential to result in total blindness and visual impairment. Despite the fact that there is no cure for RP, people can manage it using rehabilitation programs and low-vision gadgets. The purpose of this research is to characterize the expanding treatment landscape for RP, as well as the justification for advanced therapy medicinal products (ATMPs). Vitamin A supplements can help prevent the sluggish visual loss caused by a prevalent kind of RP. The presence of visual purple in the rods and the underlying vascular choroid causes the retina to look purplish red. The major portion of the retina damaged is the rod photoreceptor electric cell; the development of diverse diseases is progressive. Because of the retina's accessibility, immunological privilege, and compartmentalization, hereditary retinal diseases are amenable to cell and gene therapy. Therapeutic techniques that attempt to rescue photoreceptors (gene therapies) require the existence of non-functional target cells, but other therapies (cell therapies) do not require the presence of live photoreceptors. To provide successful therapy choices for RP patients at all disease phases, the development pipeline must be continually diversified and advanced, as well as ongoing efforts to encourage early patient identification and quick diagnosis. Future research will focus on avoiding vision loss in genetic eye illnesses and assisting patients in regaining their eyesight. Retinal implants, cell therapies, supplementary medications, and gene therapies may become common treatments for reducing vision loss in the future. Cureus 2023-10-30 /pmc/articles/PMC10686897/ /pubmed/38034182 http://dx.doi.org/10.7759/cureus.48006 Text en Copyright © 2023, Kamde et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pathology
Kamde, Saakshi P
Anjankar, Anil
Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title_full Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title_fullStr Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title_full_unstemmed Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title_short Retinitis Pigmentosa: Pathogenesis, Diagnostic Findings, and Treatment
title_sort retinitis pigmentosa: pathogenesis, diagnostic findings, and treatment
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686897/
https://www.ncbi.nlm.nih.gov/pubmed/38034182
http://dx.doi.org/10.7759/cureus.48006
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