Results 91 to 100 of about 4,867,114 (192)

Stargardt disease caused by a rare combination of double homozygous mutations [PDF]

, 2013
Stargardt disease is a juvenile macular degeneration most often inherited in an autosomal recessive pattern, characterized by decreased vision in the first 2 decades of life. This report presents a clinical case of Stargardt disease: a 10-year-old female
Serapinas, Danielius, Raimundas Sakalauskas, Laukaitienė, Viltautė, Sakalauskas, Raimundas, Danielius Serapinas, Viltautė Obrikytė   +5 more
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Early-onset stargardt disease: phenotypic and genotypic characteristics

, 2015
Item does not contain fulltextOBJECTIVE: To describe the phenotype and genotype of patients with early-onset Stargardt disease. DESIGN: Retrospective cohort study.
Bax, N.M., Klevering, B.J., Lambertus, S., Huet, R.A.C. van, Hoefsloot, L.H., Cremers, F.P.M., Boon, C.J.F., Hoyng, C.B.   +7 more
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Fixation Improvement through Biofeedback Rehabilitation in Stargardt Disease

Case Reports in Medicine, 2016
Stargardt disease is the most common hereditary macular degeneration in juveniles. It is characterized by macular dystrophy associated with loss of central vision in the first or second decade of life, a “beaten-metal” appearance in the fovea or ...
G. Scuderi, F. Verboschi, D. Domanico, L. Spadea   +3 more
doaj   +1 more source

Choroidal Thickness in Different Types of Inherited Retinal Dystrophies

Journal of Ophthalmic & Vision Research, 2020
Purpose: To compare the choroidal thickness among eyes with retinitis pigmentosa (RP), Stargardt disease, Usher syndrome, cone-rod dystrophy, and healthy eyes of sex- and age-matched individuals. Methods: In this comparative study, 503 eyes with RP
Hamideh Sabbaghi, Hamid Ahmadieh, Jalil Jalili, Nazanin Behnaz, Maryam Fakhri, Fatemeh Suri, Bahareh Kheiri, Mojtaba Rajabpour, Morteza Entezari, Narsis Daftarian   +9 more
doaj   +1 more source

Macular hyperpigmentary changes in ABCA4-Stargardt disease

International Journal of Retina and Vitreous, 2019
Background Stargardt disease (STGD) and age-related macular degeneration (AMD) share clinical and pathophysiological features. In AMD, macular hyperpigmentary changes are associated to a worse prognosis.
Maria Fernanda Abalem, Amro A. Omari, Dana Schlegel, Naheed W. Khan, Thiran Jayasundera   +4 more
doaj   +1 more source

Deep Learning to Distinguish ABCA4-Related Stargardt Disease from PRPH2-Related Pseudo-Stargardt Pattern Dystrophy

, 2021
(1) Background: Recessive Stargardt disease (STGD1) and multifocal pattern dystrophy simulating Stargardt disease (“pseudo-Stargardt pattern dystrophy”, PSPD) share phenotypic similitudes, leading to a difficult clinical diagnosis.
Olivia Zambrowski, Francesca Amoroso, Carl-Joe Mehanna, Carlotta Pallone, Arthur Kessler, Eric Petit, Paul Denys, Eric H. Souied, Alexandra Miere, Daniel Seknazi   +9 more
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New Insights Into Stargardt Disease With Multimodal Imaging

, 2015
A 20-year-old woman with bilateral mild blurring of vision presented with a bull\u27s eye maculopathy and was diagnosed with Stargardt disease, confirmed with genetic testing.
Sherman, J., Suqin, Y., Yu Suqin, Jerome Sherman, Freund, K. B., Claudine E. Pang, K. Bailey Freund, Pang, C. E.   +7 more
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Facts about stargardt disease: advances and obstacles [PDF]

, 2016
Department of Ophthalmology, Nicolae Testemitanu State University of Medicine and Pharmacy, Chisinau, Republic of Moldova, The 6th International Medical Congress for Students and Young Doctors, May 12-14, 2016Introduction: Stargardt disease is the ...
Pavlovschi, Ecaterina, Bilba, Rodica, Turcanu, Irina, Borovic, Djina   +3 more
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Fundus Autofluorescence in Inherited Retinal Disease: A Review

Cells
Fundus autofluorescence (FAF) is a non-invasive retinal imaging technique that helps visualize naturally occurring fluorophores, such as lipofuscin, and provides valuable insight into retinal diseases—particularly inherited retinal diseases (IRDs).
Jin Kyun Oh, Omar Moussa, Byron L. Lam, Jesse D. Sengillo   +3 more
doaj   +1 more source

Clinical classification of Stargardt disease. [PDF]

Graefes Arch Clin Exp Ophthalmol, 2023
Contains fulltext : 305742.pdf (Publisher’s version ) (Open Access)
Pas JAAH, Dhooge PPA, Hoyng CB.
europepmc   +5 more sources