X-Linked Retinal Dysplasia Latest Advances

Find the Latest Research About X-Linked Retinal Dysplasia

Last Updated: 06/30/2026

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Found 650 publications

Retrospective evaluation of the prevalence of known and presumed hereditary eye diseases in a population of Labradoodles referred for ophthalmic screening examinations in the Netherlands.

Retrospective evaluation of the prevalence of known and presumed hereditary eye diseases in a population of Labradoodles referred for ophthalmic screening examinations in the Netherlands.

Journal: Frontiers in veterinary science

Published: March 29, 2026

Comparison of Presumed Geographic Retinal Dysplasia Between a Cavalier King Charles Spaniel and a Labrador Retriever.

Comparison of Presumed Geographic Retinal Dysplasia Between a Cavalier King Charles Spaniel and a Labrador Retriever.

Journal: Clinical case reports

Published: January 05, 2026

Neonatal Purpura Fulminans: An Unusual Cause of Leukocoria, Retinal Detachment, and Vitreous Hemorrhage in Neonates.

Neonatal Purpura Fulminans: An Unusual Cause of Leukocoria, Retinal Detachment, and Vitreous Hemorrhage in Neonates.

Journal: Cureus

Published: December 27, 2025

Dysfunctional CRPPA is responsible for recessively inherited Hereford hydrocephalus with muscular dystrophy and retinal dysplasia.

Dysfunctional CRPPA is responsible for recessively inherited Hereford hydrocephalus with muscular dystrophy and retinal dysplasia.

Journal: Veterinary pathology

Published: October 09, 2025

Investigating motile ciliopathies in a pediatric case of an abnormal optic nerve head.

Investigating motile ciliopathies in a pediatric case of an abnormal optic nerve head.

Journal: Ophthalmic genetics

Published: September 03, 2025

Congenital Ocular Findings in an Antillean Manatee (Trichechus manatus manatus).

Congenital Ocular Findings in an Antillean Manatee (Trichechus manatus manatus).

Journal: Veterinary medicine and science

Published: August 10, 2025

Deletion of versican V0/V2 isoforms in mice leads to retinal dysplasia.

Deletion of versican V0/V2 isoforms in mice leads to retinal dysplasia.

Journal: Experimental eye research

Published: July 24, 2025

Ophthalmologic manifestations associated with Fukutin (FKTN) variant subtypes in Korean patients with Fukuyama congenital muscular dystrophy: a single-center retrospective case series.

Ophthalmologic manifestations associated with Fukutin (FKTN) variant subtypes in Korean patients with Fukuyama congenital muscular dystrophy: a single-center retrospective case series.

Journal: BMC ophthalmology

Published: July 14, 2025

Fukuyama congenital muscular dystrophy: Clinical features and therapeutic advances.

Fukuyama congenital muscular dystrophy: Clinical features and therapeutic advances.

Journal: Brain & development

Published: May 18, 2025

Early-Onset Retinal Dysfunction Associated with Novel WDR19 Variants in Sensenbrenner Syndrome.

Early-Onset Retinal Dysfunction Associated with Novel WDR19 Variants in Sensenbrenner Syndrome.

Journal: Diagnostics (Basel, Switzerland)

Published: May 11, 2025

Nonrandomized Allocation of Steroid Therapy in Patients With Fukuyama Congenital Muscular Dystrophy: Study Protocol for a Phase II Clinical Trial.

Nonrandomized Allocation of Steroid Therapy in Patients With Fukuyama Congenital Muscular Dystrophy: Study Protocol for a Phase II Clinical Trial.

Journal: Neuropsychopharmacology reports

Published: February 24, 2025

Cross-Sectional Study of the Association Between Plasma Brain Natriuretic Peptide Levels and Left Ventricular Shortening Fraction in Fukuyama Congenital Muscular Dystrophy.

Cross-Sectional Study of the Association Between Plasma Brain Natriuretic Peptide Levels and Left Ventricular Shortening Fraction in Fukuyama Congenital Muscular Dystrophy.

Journal: The Tohoku journal of experimental medicine

Published: November 20, 2024

Showing 1-12 of 650

Last Updated: 06/30/2026