Cargando…

Functional Analysis of Retinal Flecks in Stargardt Disease

PURPOSE: To evaluate visual function of flecked areas in a series of patients with Stargardt disease (STGD) and compare them with adjacent non flecked areas. METHODS: Twenty–seven patients with STGD, ABCA4 mutations and yellowish retinal flecks at fundus examination were recruited. Microperimetry wi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Verdina, Tommaso, Tsang, Stephen H., Greenstein, Vivienne C., Zernant, Jana, Sodi, Andrea, Lima, Luiz H., Chang, Stanley, Allikmets, Rando, Menchini, Ugo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2012
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882688/ https://www.ncbi.nlm.nih.gov/pubmed/24409374 http://dx.doi.org/10.4172/2155-9570.1000233

Ejemplares similares

Familial discordance in Stargardt disease
por: Burke, Tomas R., et al.
Publicado: (2012)

Retinal Pigment Epithelium Atrophy in Recessive Stargardt Disease as Measured by Short-Wavelength and Near-Infrared Autofluorescence
por: Jauregui, Ruben, et al.
Publicado: (2021)

Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
por: Su, Pei-Yin, et al.
Publicado: (2022)

Penetrance of the ABCA4 p.Asn1868Ile Allele in Stargardt Disease
por: Allikmets, Rando, et al.
Publicado: (2018)

Comparisons Among Optical Coherence Tomography and Fundus Autofluorescence Modalities as Measurements of Atrophy in ABCA4-Associated Disease
por: Parmann, Rait, et al.
Publicado: (2022)

A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease
por: Greenstein, Vivienne C., et al.
Publicado: (2017)

Extremely hypomorphic and severe deep intronic variants in the ABCA4 locus result in varying Stargardt disease phenotypes
por: Zernant, Jana, et al.
Publicado: (2018)

Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence
por: Greenstein, Vivienne C., et al.
Publicado: (2023)

A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
por: Kolesnikova, Masha, et al.
Publicado: (2022)

RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIME
por: Solberg, Yasmin, et al.
Publicado: (2019)

Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt disease
por: Charng, Jason, et al.
Publicado: (2020)

Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease
por: Fujinami, Kaoru, et al.
Publicado: (2014)

Progressive Choriocapillaris Impairment in ABCA4 Maculopathy Is Secondary to Retinal Pigment Epithelium Atrophy
por: Jauregui, Ruben, et al.
Publicado: (2020)

Clinical and genetic findings in Italian patients with sector retinitis pigmentosa
por: Verdina, Tommaso, et al.
Publicado: (2021)

Dietary profile of patients with Stargardt’s disease and Retinitis Pigmentosa: is there a role for a nutritional approach?
por: Sofi, Francesco, et al.
Publicado: (2016)

Correlation of Morphology and Function of Flecks Using Short-Wave Fundus Autofluorescence and Microperimetry in Patients With Stargardt Disease
por: Dhooge, Patty P. A., et al.
Publicado: (2021)

Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease
por: Zernant, Jana, et al.
Publicado: (2022)

A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes
por: Lee, Winston, et al.
Publicado: (2022)

Shared Features in Retinal Disorders With Involvement of Retinal Pigment Epithelium
por: Sparrow, Janet R., et al.
Publicado: (2021)

Simultaneous Expression of ABCA4 and GPR143 Mutations: A Complex Phenotypic Manifestation
por: Lee, Winston, et al.
Publicado: (2016)

Insights Into PROM1-Macular Disease Using Multimodal Imaging
por: Paavo, Maarjaliis, et al.
Publicado: (2023)

Late-onset pattern macular dystrophy mimicking ABCA4 and PRPH2 disease is caused by a homozygous frameshift mutation in ROM1
por: Ma, Chu Jian, et al.
Publicado: (2019)

Mutations in GPR143/OA1 and ABCA4 Inform Interpretations of Short-Wavelength and Near-Infrared Fundus Autofluorescence
por: Paavo, Maarjaliis, et al.
Publicado: (2018)

Benign fleck retina
por: Mohan, Sashwanthi, et al.
Publicado: (2022)

Choroidal Caverns in Stargardt Disease
por: Mucciolo, Dario Pasquale, et al.
Publicado: (2022)

Morphology of the Leather Defect Light Flecks and Spots
por: Nafstad, O, et al.
Publicado: (2001)

Choroideremia Carriers: Dark-Adapted Perimetry and Retinal Structures
por: Parmann, Rait, et al.
Publicado: (2022)

Genetic and Clinical Analysis of ABCA4-Associated Disease in African American Patients
por: Zernant, Jana, et al.
Publicado: (2014)

EDI OCT evaluation of choroidal thickness in Stargardt disease
por: Sodi, Andrea, et al.
Publicado: (2018)

Ein heller Fleck beim Lesen
por: Farghaly, Louisa, et al.
Publicado: (2023)

Quantifying Fundus Autofluorescence in Patients With Retinitis Pigmentosa
por: Schuerch, Kaspar, et al.
Publicado: (2017)

Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod Dystrophy
por: Collison, Frederick T., et al.
Publicado: (2019)

Corneal Fleck dystrophy in a Spanish family
por: Rocha-de-Lossada, Carlos, et al.
Publicado: (2020)

Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants
por: Katagiri, Satoshi, et al.
Publicado: (2018)

Multi-platform imaging in ABCA4-Associated Disease
por: Chen, Lijuan, et al.
Publicado: (2019)

Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients
por: Sodi, Andrea, et al.
Publicado: (2011)

Variation in the Level of Grain Defect Light Flecks and Spots on Cattle Hides
por: Nafstad, O, et al.
Publicado: (2001)

A novel PIKFYVE mutation in fleck corneal dystrophy
por: Kotoulas, Andreas, et al.
Publicado: (2011)

Multi-modal imaging in benign familial fleck retina
por: Kumar, Nitin, et al.
Publicado: (2021)

Hyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal Degeneration
por: Sengillo, Jesse D., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_1p1fk0dc1bja96jeqsd7efkt97