Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Inherited retinal degenerations: clinical phenotypes and emerging therapies.

Lancet (London, England) - 25 Jul 2026

Uyhazi Katherine E, O'Neil Erin C, Aleman Tomas S, Cideciyan Artur V

Abstract excerpt

Inherited retinal degenerations are a diverse group of genetic disorders that result in progressive vision loss. Advances in genetic testing have revealed pathogenic variants in hundreds of genes, reflecting the remarkable heterogeneity of these conditions and pointing to the complexity of the developmental and homoeostatic processes needed for a lifetime of good vision. This Review summarises the clinical...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Therapy
Share to Phenotype
Share to Retinal Degeneration

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 42409034
DOI: 10.1016/S0140-6736(26)00766-X

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 15 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited retinal degenerations: clinical phenotypes and emerging therapies.PMID 42409034Read ↗

Inherited retinal diseases: Therapeutics, clinical trials and end points—A reviewSemantic proximity Read ↗

State of the Art on Inherited Retinal Dystrophies: Management and Molecular GeneticsSemantic proximity Read ↗

Gene Therapy for Inherited Retinal Diseases: From Laboratory Bench to Patient Bedside and BeyondSemantic proximity Read ↗

Retinitis pigmentosa: recent advances and future directions in diagnosis and managementSemantic proximity Read ↗

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes.Semantic proximity Read ↗

Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities.Semantic proximity Read ↗

Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups.Semantic proximity Read ↗

Gene-agnostic approaches to treating inherited retinal degenerationsSemantic proximity Read ↗

Genetics in Retinal Diseases.Semantic proximity Read ↗

History of Finding Genes and Mutations Causing Inherited Retinal Diseases.Semantic proximity Read ↗

Emerging therapies for inherited retinal degeneration.Semantic proximity Read ↗

Hereditary retinal disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.