Bilateral exudative retinal detachments after subretinal gene therapy with voretigene neparvovec-rzyl for RPE65 Leber Congenital Amaurosis

Bilateral exudative retinal detachments after subretinal gene therapy with voretigene neparvovec-rzyl for RPE65 Leber Congenital Amaurosis

Purpose: To report panuveitis with exudative retinal detachments in a healthy 27-year-old woman with biallelic mutations in the RPE65 gene, who underwent bilateral sequential gene therapy with subretinal administration of voretigene neparvovec-rzyl. Observations: Visual acuity improved for 30 days a...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron:	Alcina K. Lidder, Stephanie Choi, Yasha S. Modi, Scott E. Brodie, Janet L. Davis, Ninel Z. Gregori, Byron L. Lam
Fformat:	Erthygl
Iaith:	English
Cyhoeddwyd:	Elsevier 2023-12-01
Cyfres:	American Journal of Ophthalmology Case Reports
Pynciau:	Subretinal gene therapy Leber congenital amaurosis Vogt-koyanagi-harada disease Sympathetic ophthalmia RPE65-Associated inherited retinal disease Panuveitis
Mynediad Ar-lein:	http://www.sciencedirect.com/science/article/pii/S2451993623000877

Eitemau Tebyg

Voretigene Neparvovec and Gene Therapy for Leber’s Congenital Amaurosis: Review of Evidence to Date
gan: Padhy SK, et al.
Cyhoeddwyd: (2020-11-01)

Características de pacientes con enfermedad de Vogt Koyanagi Harada del departamento de reumatología del Hospital de Clínicas
gan: Jhonatan Losanto, et al.
Cyhoeddwyd: (2017-03-01)

Síndrome de Vogt-Koyanagi-Harada
gan: Juan Carlos Serna-Ojeda, et al.
Cyhoeddwyd: (2016-07-01)

Síndrome de Vogt-Koyanagi-Harada
gan: Juan Carlos Serna-Ojeda, et al.
Cyhoeddwyd: (2016-07-01)

A rare pediatric case of probable Vogt–Koyanagi–Harada syndrome
gan: Malarvizhi Raman, et al.
Cyhoeddwyd: (2019-01-01)

Unusual Case of Vogt-Koyanagi-Harada Syndrome Presenting as Non-specific Headache
gan: Pradeep A.V., et al.
Cyhoeddwyd: (2014-04-01)

Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis
gan: Maximilian J. Gerhardt, et al.
Cyhoeddwyd: (2022-12-01)

Vogt-Koyanagi-Harada disease presenting secondary to a post-infectious Mycoplasma pneumoniae autoimmune response
gan: Christian I. Wade, MD, et al.
Cyhoeddwyd: (2020-09-01)

Seven novel variants expand the spectrum of RPE65-related Leber congenital amaurosis in the Chinese population
gan: Zilin Zhong, et al.
Cyhoeddwyd: (2019-03-01)

A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis
gan: Jing Liu, et al.
Cyhoeddwyd: (2017-01-01)

Prospective study of clinical characteristics and visual outcome in vogt–koyanagi–Harada syndrome in a tertiary eye hospital in South India
gan: Saranya Balakrishnan, et al.
Cyhoeddwyd: (2023-01-01)

Vogt Koyanagi Harada syndrome in a 15-year-old girl, steroids side effects and recurrences
gan: Gamze Yıldırım, et al.
Cyhoeddwyd: (2021-06-01)

VKH disease in the elderly: Variations in clinical course as compared to VKH disease in adults
gan: Hrishikesh Kaza, et al.
Cyhoeddwyd: (2024-01-01)

Sympathetic Ophthalmia: Demographic Characteristics, Clinical Findings, and Treatment Results
gan: Kübra Özdemir Yalçınsoy, et al.
Cyhoeddwyd: (2023-02-01)

A Case of Vogt-Koyanagi-Harada Disease-Like Uveitis Induced by Nivolumab and Ipilimumab Combination Therapy
gan: Keisuke Minami, et al.
Cyhoeddwyd: (2021-12-01)

Could internal limiting membrane peeling before Voretigen neparvovec-ryzl subretinal injection prevent focal chorioretinal atrophy?
gan: Lea Dormegny, et al.
Cyhoeddwyd: (2024-02-01)

Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
gan: Masha Kolesnikova, et al.
Cyhoeddwyd: (2022-11-01)

Espectro Clínico y Biomarcadores Genéticos de susceptibilidad en el síndrome de Vogt-Koyanagi- Harada en pacientes Paraguayos
gan: Nelly Colmán, et al.
Cyhoeddwyd: (2021-06-01)

Voretigene Neparvovec in Retinal Diseases: A Review of the Current Clinical Evidence
gan: Gao J, et al.
Cyhoeddwyd: (2020-11-01)

Assessing the Accuracy, Quality, and Readability of Patient Accessible Online Resources Regarding Ocular Gene Therapy and Voretigene Neparvovec
gan: Davuluri S, et al.
Cyhoeddwyd: (2021-09-01)

The effect of human gene therapy for RPE65-associated Leber’s congenital amaurosis on visual function: a systematic review and meta-analysis
gan: Xue Wang, et al.
Cyhoeddwyd: (2020-02-01)

Commentary on “Vogt–Koyanagi–Harada Syndrome Following COVID-19 mRNA Vaccination: Th2 to Th1 Transition-related Molecular Machinery”
gan: Hinpetch Daungsupawong, et al.
Cyhoeddwyd: (2024-09-01)

Bilateral Iris depigmentation, transillumination defects and hypotony in Vogt–Koyanagi–Harada disease
gan: Mohit Garg, et al.
Cyhoeddwyd: (2022-01-01)

Presentation of sclerouveitis with features of Vogt Koyanagi Harada syndrome and ocular tuberculosis – A Rare Combination
gan: Purva Vijay Deore, et al.
Cyhoeddwyd: (2022-01-01)

The Role of TRiC-enhanced Actin Folding in Leber Congenital Amaurosis
gan: Silke Berger, et al.
Cyhoeddwyd: (2023-02-01)

A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy
gan: Hane Lee, et al.
Cyhoeddwyd: (2025-01-01)

Publication trends of Leber congenital amaurosis researches: a bibliometric study during 2002-2022
gan: Xiao-Xu Huang, et al.
Cyhoeddwyd: (2024-08-01)

Vogt–Koyanagi–Harada syndrome – current perspectives
gan: Baltmr A, et al.
Cyhoeddwyd: (2016-11-01)

Leber’s congenital amaurosis and the role of gene therapy in congenital retinal disorders
gan: Walid Sharif, et al.
Cyhoeddwyd: (2017-03-01)

Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9
gan: Mostafa Neissi, et al.
Cyhoeddwyd: (2024-10-01)

Vogt-Koyanagi-Harada-Like Uveitis Secondary to Pembrolizumab in Metastatic Gastric Cancer: A Case Report and Review of the Literature
gan: Ryan A. Denu, et al.
Cyhoeddwyd: (2024-09-01)

Three mb. Vogt-koyanagi-harada cases in Slovenia
gan: Nataša Vidovič-Valentinčič, et al.
Cyhoeddwyd: (2005-10-01)

Vogt-Koyanagi-Harada Syndrome in a 10 Years Old Child.
gan: Aalia R Sufi, et al.
Cyhoeddwyd: (2011-07-01)

Vogt-Koyanagi-Harada disease: a retrospective and multicentric study of 41 patients
gan: K. Diallo, et al.
Cyhoeddwyd: (2020-10-01)

Ocular syphilis mimicking Vogt–Koyanagi–Harada disease
gan: Yu-Ching Lin, et al.
Cyhoeddwyd: (2019-01-01)

A rare case of Vogt–Koyanagi–Harada disease presenting simultaneously with pituitary macroadenoma
gan: Pradeep Kumar Panigrahi
Cyhoeddwyd: (2022-01-01)

Adalimumab como alternativa terapéutica en el síndrome de Vogt Koyanagi Harada refractario al infliximab: reporte de caso
gan: Eugenio Franklin Moya Ayre, et al.
Cyhoeddwyd: (2016-03-01)

Intraocular Lens Dislocation into the Anterior Chamber because of Repeated Eye-Poking in a Patient with Leber’s Congenital Amaurosis
gan: Abdullah A. Al-Owaid, et al.
Cyhoeddwyd: (2020-01-01)

A novel RPE65 variant p.(Ala391Asp) in Leber congenital amaurosis: a case report and literature review in Japan
gan: Natsuki Higa, et al.
Cyhoeddwyd: (2024-09-01)

Bilateral optic disc edema and serous retinal detachment as initial ocular manifestations of systemic lymphoma: A case report and literature review
gan: Chi-Yeh Wu, et al.
Cyhoeddwyd: (2023-04-01)