Results 171 to 180 of about 10,317 (215)
Censoring the Floor Effect in Long-Term Stargardt Disease Microperimetry Data Produces a Faster Rate of Decline. [PDF]
Ophthalmol SciCharng J +6 more
europepmc +1 more source
Presentation and Clinical Features of Stargardt Disease in a Series of Nigerian Patients.
Ann Afr MedOderinlo O, Akanbi T.
europepmc +1 more source
A comparative study of choroidal structural features in eyes with central macular atrophy related to Stargardt disease and non-exudative age-related macular degeneration. [PDF]
Indian J OphthalmolBatıoğlu F +5 more
europepmc +1 more source
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Current Opinion in Ophthalmology, 2021
Purpose of review Stargardt disease is the most common inherited macular dystrophy but has a wide clinical spectrum, and several inherited macular dystrophies have phenotypic similarities that can make clinical diagnosis challenging.
Aaron M, Ricca +2 more
openaire +2 more sources
Purpose of review Stargardt disease is the most common inherited macular dystrophy but has a wide clinical spectrum, and several inherited macular dystrophies have phenotypic similarities that can make clinical diagnosis challenging.
Aaron M, Ricca +2 more
openaire +2 more sources
Georgetown Medical Review, 2022
Stargardt disease is a slowly progressing macular dystrophy with an onset of disease most commonly in children and young adults. Numerous genes have been found to be associated with this disease, with variants in the retina specific ATP- binding cassette transporter (ABCA4) gene being most common.
Kevin Delijani +5 more
openaire +2 more sources
Stargardt disease is a slowly progressing macular dystrophy with an onset of disease most commonly in children and young adults. Numerous genes have been found to be associated with this disease, with variants in the retina specific ATP- binding cassette transporter (ABCA4) gene being most common.
Kevin Delijani +5 more
openaire +2 more sources
2018
Stargardt disease (STGD) is one of the most common macular dystrophies in young adults. It progresses slowly. Its prevalence is about 1:8000-10,000. Age of onset is a surrogate marker: The earlier the onset, the more severe the disease course. Onset usually occurs in childhood or early adolescence, at about 10-15 years of age.
Stephen H, Tsang, Tarun, Sharma
+5 more sources
Stargardt disease (STGD) is one of the most common macular dystrophies in young adults. It progresses slowly. Its prevalence is about 1:8000-10,000. Age of onset is a surrogate marker: The earlier the onset, the more severe the disease course. Onset usually occurs in childhood or early adolescence, at about 10-15 years of age.
Stephen H, Tsang, Tarun, Sharma
+5 more sources
2012
Abstract Autosomal recessive Stargardt disease and fundus flavimaculatus represent a single clinical entity caused by mutation of the ABCA4 gene and accumulation of defective gene product (A2E) at the level of the RPE. The autosomal dominant STGD3 phenotype results when a mutation in the ELOVL4 gene produces a truncated protein that ...
Aimee V. Chappelow, Elias I. Traboulsi
+4 more sources
Abstract Autosomal recessive Stargardt disease and fundus flavimaculatus represent a single clinical entity caused by mutation of the ABCA4 gene and accumulation of defective gene product (A2E) at the level of the RPE. The autosomal dominant STGD3 phenotype results when a mutation in the ELOVL4 gene produces a truncated protein that ...
Aimee V. Chappelow, Elias I. Traboulsi
+4 more sources
Documenta Ophthalmologica, 1992
Three families including seven members with Stargardt's disease were examined. In addition to the affected family members, 43 of the relatives had an eye examination. In one family, there was a consanguineous marriage to be found. The heredity was most probably autosomal recessive in all of the three families.
M, Mäntyjärvi, K, Tuppurainen
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Three families including seven members with Stargardt's disease were examined. In addition to the affected family members, 43 of the relatives had an eye examination. In one family, there was a consanguineous marriage to be found. The heredity was most probably autosomal recessive in all of the three families.
M, Mäntyjärvi, K, Tuppurainen
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Retina, 2017
Purpose: To identify changes in the outer retina in areas without atrophy or flecks of Stargardt disease (STGD) using spectral-domain optical coherence tomography. Methods: Twenty-three STGD patients and 26 control subjects were assessed for outer retina (from the outer border of ...
Jacob G, Light +5 more
openaire +2 more sources
Purpose: To identify changes in the outer retina in areas without atrophy or flecks of Stargardt disease (STGD) using spectral-domain optical coherence tomography. Methods: Twenty-three STGD patients and 26 control subjects were assessed for outer retina (from the outer border of ...
Jacob G, Light +5 more
openaire +2 more sources