Cargando…

Unilateral retinocytoma associated with a variant in the RB1 gene

BACKGROUND: Retinocytoma is a rare benign retinal tumor associated with variants in the RB1 gene. Ophthalmoscopic features can include a translucent retinal mass, calcification, retinal pigment epithelial alteration and chorioretinal atrophy. METHODS: Detailed ophthalmological examinations were perf...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wu, Shijing, Zou, Xuan, Sun, Zixi, Zhu, Tian, Wei, Xing, Sui, Ruifang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2020
Materias:	Clinical Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196460/ https://www.ncbi.nlm.nih.gov/pubmed/31997559 http://dx.doi.org/10.1002/mgg3.1156

Ejemplares similares

Retinocytoma associated with bilateral retinoblastoma
por: Naseripour, Masood, et al.
Publicado: (2010)

Fundus autofluorescence in retinocytoma
por: Dubey, Devashish, et al.
Publicado: (2022)

Retinocytoma: A Case Series
por: Bubshait, Luluah, et al.
Publicado: (2023)

Multimodal imaging in a case of retinocytoma
por: Temkar, Shreyas, et al.
Publicado: (2018)

Atypical retinocytoma with diffuse vitreous seeds: An insight
por: Shah, Parag K., et al.
Publicado: (2011)

Fundus fluorescein angiography in a macular retinocytoma
por: Dubey, Devashish, et al.
Publicado: (2022)

Retinocytoma Undergoing Retinoblastoma Transformation in an Adult Patient
por: Navaratnam, J., et al.
Publicado: (2023)

Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7
por: Zou, Xuan, et al.
Publicado: (2021)

Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities
por: Sun, Zixi, et al.
Publicado: (2017)

A novel small deletion in the NHS gene associated with Nance-Horan syndrome
por: Li, Huajin, et al.
Publicado: (2018)

Association of the TNF-α, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort
por: Gulel, Aslihan, et al.
Publicado: (2018)

Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism
por: Zou, Xuan, et al.
Publicado: (2017)

Deletion of Rb1 gene in late osteosarcoma from survivor of unilateral retinoblastoma--a case report.
por: Lee, S. Y., et al.
Publicado: (1996)

Mutation Spectrum of RB1 Gene in Unilateral Retinoblastoma Cases from Tunisia and Correlations with Clinical Features
por: Ayari-Jeridi, Hajer, et al.
Publicado: (2015)

To Rb or not to Rb
por: Wells, William A.
Publicado: (2002)

Complete Genome Sequences of T4-Like Bacteriophages RB3, RB5, RB6, RB7, RB9, RB10, RB27, RB33, RB55, RB59, and RB68
por: Yaung, Stephanie J., et al.
Publicado: (2015)

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration
por: Dharmat, Rachayata, et al.
Publicado: (2017)

Genetic and clinical characterization of mainland Chinese patients with sialidosis type 1
por: Han, Xiaoxu, et al.
Publicado: (2020)

Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency
por: Liu, Cheng, et al.
Publicado: (2012)

Quality of Life (QoL) and Psychosocial Outcomes in Adult Survivors of Unilateral Retinoblastoma (RB) in China
por: Feng, Yiyi, et al.
Publicado: (2020)

Posterior INFIX for Treating Unilateral Unstable Sacral Fractures
por: Qi, Haotian, et al.
Publicado: (2022)

Combination of the ginsenosides Rb3 and Rb2 exerts protective effects against myocardial ischemia reperfusion injury in rats
por: Liu, Xiaomin, et al.
Publicado: (2020)

Comprehensive multiomics analysis of the effect of ginsenoside Rb1 on hyperlipidemia
por: Lianqun, Jia, et al.
Publicado: (2021)

A Novel, Likely Pathogenic MAX Germline Variant in a Patient With Unilateral Pheochromocytoma
por: Lam-Chung, César Ernesto, et al.
Publicado: (2021)

A Review of Machine Learning Algorithms for Retinal Cyst Segmentation on Optical Coherence Tomography
por: Wei, Xing, et al.
Publicado: (2023)

Transcription of the Tumor Suppressor Genes p53 and RB in Lymphocytes from Patients with Chronic Kidney Disease: Evidence of Molecular Senescence?
por: Kordinas, Vasileios, et al.
Publicado: (2012)

The beta-decay of $^{95}$Rb and $^{97}$Rb
por: Kratz, K L, et al.
Publicado: (1983)

Unilateral Facial Weakness
por: Mohd Nasir, Mohd Zulhilmie, et al.
Publicado: (2019)

Unilateral Cervical Lymphadenopathy
por: Al Awfi, Mahmood Masud, et al.
Publicado: (2020)

RB1 Circulating Tumor DNA in the Blood of Patients with Unilateral Retinoblastoma: Before and after Intra-arterial Chemotherapy
por: Francis, Jasmine H., et al.
Publicado: (2021)

Lamina Abrasion Caused by High-Speed Drill in Unilateral Door Cervical Laminoplasty: A Clinical Investigation
por: Zou, Jiwei, et al.
Publicado: (2023)

Deep Learning with Automatic Data Augmentation for Segmenting Schisis Cavities in the Optical Coherence Tomography Images of X-Linked Juvenile Retinoschisis Patients
por: Wei, Xing, et al.
Publicado: (2023)

Unilateral Lennox–Gastaut syndrome associated with Klippel–Trénaunay syndrome
por: Tabarki, Brahim, et al.
Publicado: (2021)

Identification and validation of RB1 as an immune-related prognostic signature based on tumor mutation burdens in bladder cancer
por: Liu, Ning, et al.
Publicado: (2022)

The role of RB1 alteration and 4q12 amplification in IDH-WT glioblastoma
por: Dono, Antonio, et al.
Publicado: (2021)

Association Between Variants of the Mannose-Binding Lectin 2 Gene and Susceptibility to Sepsis in the Hainan Island
por: Cheng, Shaowen, et al.
Publicado: (2022)

Percutaneous Endoscopic Transforaminal Lumbar Discectomy via Eccentric Trepan foraminoplasty Technology for Unilateral Stenosed Serve Root Canals
por: Zou, Hong‐jun, et al.
Publicado: (2020)

A Case of Unilateral Hypertrophy
por: Simpson, B. Soutar
Publicado: (1926)

Unilateral submandibular gland agenesis
por: Indiran, Venkatraman
Publicado: (2016)

Diffuse unilateral subacute neuroretinitis
por: Ganne, Pratyusha, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_biroaiarst1optebqmm2cjtm0f