Cargando…
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...
Autores principales: | , |
---|---|
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 |
_version_ | 1785151864435638272 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10686897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kamdesaakship retinitispigmentosapathogenesisdiagnosticfindingsandtreatment AT anjankaranil retinitispigmentosapathogenesisdiagnosticfindingsandtreatment |