Cargando…

The Burden of X-Linked Retinitis Pigmentosa on Patients and Society: A Narrative Literature Review

X-linked retinitis pigmentosa (XLRP) is a severe form of retinitis pigmentosa (RP), a rare, inherited retinal degenerative disorder, that causes blindness. The aim of this literature review was to identify what is currently known about the burden of XLRP. Literature databases were searched for artic...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chivers, Marie, Li, Nan, Pan, Feng, Wieffer, Heather, Slowik, Rafal, Leartsakulpanitch, Jittrakul
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236258/ https://www.ncbi.nlm.nih.gov/pubmed/34188501 http://dx.doi.org/10.2147/CEOR.S297287

Ejemplares similares

X-Linked Retinitis Pigmentosa Gene Therapy: Preclinical Aspects
por: Mansouri, Vahid
Publicado: (2022)

Radial fundus autofluorescence in the periphery in patients with X-linked retinitis pigmentosa
por: Ogino, Ken, et al.
Publicado: (2015)

Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa
por: Zhang, Zhimeng, et al.
Publicado: (2019)

Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations
por: von Krusenstiern, Lenore, et al.
Publicado: (2023)

Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs
por: Cross, Nancy, et al.
Publicado: (2022)

Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing
por: Neidhardt, John, et al.
Publicado: (2008)

Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations
por: Di Iorio, Valentina, et al.
Publicado: (2020)

X-Linked Retinitis Pigmentosa Caused by Non-Canonical Splice Site Variants in RPGR
por: Kortüm, Friederike, et al.
Publicado: (2021)

X ‐linked inheritance of primary ciliary dyskinesia and retinitis pigmentosa due to RPGR variant: A case report and literature review
por: Kuroda, Aoi, et al.
Publicado: (2023)

The Management of “Coats' Response” in a Patient with X-Linked Retinitis Pigmentosa—A Case Report
por: Bansal, Shveta, et al.
Publicado: (2011)

The X-linked Retinitis Pigmentosa protein RP2 facilitates traffic of cilia target proteins
por: Schwarz, N, et al.
Publicado: (2012)

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers
por: Kurata, Kentaro, et al.
Publicado: (2019)

Analysis of RP2 and RPGR Mutations in Five X-Linked Chinese Families with Retinitis Pigmentosa
por: Jiang, Jingjing, et al.
Publicado: (2017)

Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel
por: Birch, David G., et al.
Publicado: (2023)

Retinitis pigmentosa
por: Hamel, Christian
Publicado: (2006)

Optical coherence tomography angiography in retinitis pigmentosa: A narrative review
por: Lu, Bingwen, et al.
Publicado: (2022)

Photoreceptor Rescue by an Abbreviated Human RPGR Gene in a Murine Model of X-linked Retinitis Pigmentosa
por: Pawlyk, Basil S., et al.
Publicado: (2015)

Novel splice receptor-site mutation of RPGR in a Chinese family with X-linked retinitis pigmentosa
por: Wang, Jing, et al.
Publicado: (2018)

Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant
por: Strubbe, Ine, et al.
Publicado: (2021)

Retinal detachment in retinitis pigmentosa
por: Chan, Weng Onn, et al.
Publicado: (2020)

Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutants
por: Ploier, Birgit, et al.
Publicado: (2016)

Retinitis Pigmentosa Masquerades: Case Series and Review of the Literature
por: Thenappan, Abinaya, et al.
Publicado: (2023)

Decoding retinitis pigmentosa
por: Natarajan, Sundaram
Publicado: (2013)

On the Heredity of Retinitis Pigmentosa
por: Schmidt, Herman
Publicado: (1875)

The Genetic Basis of Pericentral Retinitis Pigmentosa—A Form of Mild Retinitis Pigmentosa
por: Comander, Jason, et al.
Publicado: (2017)

Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa
por: Koller, Samuel, et al.
Publicado: (2023)

RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHY
por: Raparia, Eva, et al.
Publicado: (2023)

Vitamins and Mineral Supplements for Retinitis Pigmentosa
por: Zhao, Ying, et al.
Publicado: (2019)

Retinal cell transplantation in retinitis pigmentosa
por: Tezel, Tongalp H., et al.
Publicado: (2021)

SLC7A14 linked to autosomal recessive retinitis pigmentosa
por: Jin, Zi-Bing, et al.
Publicado: (2014)

Retinal gene therapy in X-linked retinitis pigmentosa caused by mutations in RPGR: Results at 6 months in a first in human clinical trial
por: Cehajic-Kapetanovic, Jasmina, et al.
Publicado: (2020)

Asymmetric presentation with a novel RP2 gene mutation in X-Linked retinitis pigmentosa: a case report
por: Lee, Hyun Woo, et al.
Publicado: (2023)

Isolated microspherophakia with retinitis pigmentosa
por: Gupta, Gaurav, et al.
Publicado: (2019)

Cataract surgery in retinitis pigmentosa
por: Chatterjee, Samrat, et al.
Publicado: (2021)

Gene therapy for retinitis pigmentosa
por: Piri, Niloofar, et al.
Publicado: (2021)

Retinitis Pigmentosa in Onitsha, Nigeria
por: Nwosu, Sebastian N. N., et al.
Publicado: (2020)

A Case of Retinitis Pigmentosa
por: Payne, Frederick W.
Publicado: (1888)

Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity
por: Obuća, Mina, et al.
Publicado: (2022)

Sector retinitis pigmentosa: Report of ten cases and a review of the literature
por: Coussa, Razek Georges, et al.
Publicado: (2019)

Allelic Heterogeneity and Genetic Modifier Loci Contribute to Clinical Variation in Males with X-Linked Retinitis Pigmentosa Due to RPGR Mutations
por: Fahim, Abigail T., et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_m3qvjhm3efr9is2ag67dgrm2g0