Gyrate Atrophy of the Choroid and Retina Latest Advances
Find the Latest Research About Gyrate Atrophy of the Choroid and Retina
Last Updated: 06/30/2026
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Found 437 publications
Macular neovascularization in patients with Gyrate atrophy.
Journal: Ophthalmic genetics
Published: June 01, 2026
Letter to the editor: Newborn screening for low blood citrulline leads to diagnosis of ornithine aminotransferase deficiency.
Journal: Molecular genetics and metabolism
Published: April 03, 2026
Intraocular Lens Opacification in a Patient With Gyrate Atrophy With a Subluxated Intraocular Lens.
Journal: The American journal of case reports
Published: January 03, 2026
Current Insight into Human Ornithine Aminotransferase: A Review.
Journal: Proteins
Published: December 23, 2025
Ultra-widefield color and autofluorescence imaging in gyrate atrophy
Journal: Journal francais d'ophtalmologie
Published: November 14, 2025
Beyond Ornithine Metabolism in Gyrate Atrophy: Tissue-Specific Proteomic Insights into Neonatal and Adult OAT Deficiency.
Journal: bioRxiv : the preprint server for biology
Published: September 26, 2025
Inborn Errors of Metabolism: Gyrate Atrophy.
Journal: Advances in experimental medicine and biology
Published: July 30, 2025
Macular Hole-Related Retinal Detachment in Gyrate Atrophy.
Journal: Retina (Philadelphia, Pa.)
Published: July 01, 2025
Gyrate Atrophy of the Choroid and Retina Diagnosed in Adulthood With a Homozygous OAT Variant: A Case Report Highlighting the Need for Long-Term Care.
Journal: Case reports in ophthalmological medicine
Published: June 17, 2025
Gyrate atrophy of the choroid and retina: a tertiary center experience.
Journal: Orphanet journal of rare diseases
Published: June 06, 2025
C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy.
Journal: Ophthalmic genetics
Published: May 14, 2025
Last Updated: 06/30/2026