Results 31 to 40 of about 109,135 (259)

Gyrate Atrophy and Choroidal Neovascularization [PDF]

Archives of Ophthalmology, 1996
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Marano, F., Deutman, A.F., Pinckers, A.J.L.G., Aandekerk, A.L.   +3 more
openaire   +3 more sources

Optical coherence tomography angiography of astrocytic hamartoma demonstrates intrinsic vascularity

American Journal of Ophthalmology Case Reports, 2020
Purpose: To evaluate the findings of astrocytic hamartoma in the setting of gyrate atrophy, including details of optical coherence tomography angiography (OCTA).
Ryan N. Vogel, T.Y. Alvin Liu, Mandeep S. Singh, Morton F. Goldberg   +3 more
doaj   +1 more source

Double macular hole with gyrate atrophy: A long-term postoperative follow-up

Journal of Clinical Ophthalmology and Research, 2022
A 55-year-old female presented with diminution of vision, night blindness, and gyrate atrophy with “double macular hole” in the left eye. Spectral-domain optical coherence tomography of the left eye showed coexisting full thickness and lamellar macular ...
Paurnima Ulhas Bodhankar, Ajit Kamalakar Joshi, Abhinandan N Patil   +2 more
doaj   +1 more source

A cohort study of 19 patients with gyrate atrophy of the choroid and retina (GACR) [PDF]

Graefe's Archive for Clinical and Experimental Ophthalmology
Roselie Diederen, Berith M Balfoort, Filip van den Broeck   +2 more
exaly   +2 more sources

Regression of macular edema with topical brinzolamide and nepafenac alone and identification of a novel gyrate atrophy mutation. [PDF]

Arq Bras Oftalmol, 2020
Gyrate atrophy is a rare metabolic autosomal recessive disorder caused by ornithine aminotransferase enzyme deficiency that leads to characteristic progressive, degenerative chorioretinal findings. Patients complain mostly of low vision, night blindness,
Çavdarlı C, Şahlı E, Çavdarlı B, Alp MN.   +3 more
europepmc   +3 more sources

Ultra-wide field imaging of an operated macular hole in gyrate atrophy [PDF]

Journal of Ophthalmic & Vision Research, 2016
Koushik Tripathy, Yog Raj Sharma, Rohan Chawla, Shreyans Jain, Alkananda Behera   +4 more
doaj   +2 more sources

Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant. [PDF]

Int J Mol Sci, 2021
We present a long-term follow-up in autosomal dominant gyrate atrophy-like choroidal dystrophy (adGALCD) and propose a possible genotype/phenotype correlation. Ophthalmic examination of six patients from two families revealed confluent areas of choroidal
Kellner U, Weisschuh N, Weinitz S, Farmand G, Deutsch S, Kortüm F, Mazzola P, Schäferhoff K, Marino V, Dell'Orco D.   +9 more
europepmc   +2 more sources

sj-docx-1-ejo-10.1177_11206721231178147 - Supplemental material for Clinical characteristics of gyrate atrophy compared with a gyrate atrophy-like retinal phenotype

, 2023
Supplemental material, sj-docx-1-ejo-10.1177_11206721231178147 for Clinical characteristics of gyrate atrophy compared with a gyrate atrophy-like retinal phenotype by L. Pauleikhoff, N. Weisschuh, A. Lentzsch, G. Spital, T. U. Krohne, H. Agostini and C.A.
H. Agostini (15847452), N. Weisschuh (15847440), G. Spital (15847446), C.A.K. Lange (15847455), A. Lentzsch (15847443), T. U. Krohne (15847449), L. Pauleikhoff (15847437)   +6 more
core   +1 more source

Gyrate Atrophy

Güncel Retina Dergisi (Current Retina Journal), 2021
Gyrate Atrophy is an autosomal recessively inherited rare disease of the choroid and retina. Deficiency of ornithine aminotransferase enzyme (OAT) leads to 10 to 20 times ornithine levels in plasma which is thought to be the cause for the ocular findings.
openaire   +1 more source

Unique case of gyrate atrophy with a well-preserved electroretinogram (ERG). [PDF]

BMJ Case Rep, 2018
Gyrate atrophy is a rare autosomal recessive disorder caused by a mutation in the ornithine-δ-Amino transferase gene. We present an interesting case of a 33-year-old woman who presented with increasing myopia, nyctalopia and failing vision.
Jasani KM, Parry NRA, Black G, Kelly SP.
europepmc   +2 more sources