Disease: Cone dystrophy
- <em>ABCA4</em>-related retinopathies in Lebanon
- <em>PRPH2</em>-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish Cohort
- <em>RTN4IP1</em>-associated non-syndromic optic neuropathy and rod-cone dystrophy
- "The Saddest Waste" - Disability, Heredity, and the Artist's Eye
- A CASE OF ALSTROM SYNDROME WITH A NOVEL VARIANT IN ALMS1 GENE PRESENTING WITH CONE ROD DYSTROPHY AS FIRST FINDING
- A diagnostic conundrum in Bardet-Biedl syndrome: when genetic diagnosis precedes clinical diagnosis
- A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcysts
- A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease
- Adaptive Optics
- Adaptive Optics Retinal Imaging in RDH12-Associated Early Onset Severe Retinal Dystrophy
- Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series
- Advanced Immunolabeling Method for Optical Volumetric Imaging Reveals Dystrophic Neurites of Dopaminergic Neurons in Alzheimer's Disease Mouse Brain
- Aland Island Eye Disease with Retinoschisis in the Clinical Spectrum of <em>CACNA1F</em>-Associated Retinopathy-A Case Report
- Alström's Syndrome, Leber's Hereditary Optic Neuropathy, or Retinitis Pigmentosa? A Case of Misdiagnosis
- An incipient late-onset retinal degeneration with a C1QTNF5 mutation: a case report with an 11-year follow-up
- Application of Electrophysiology in Non-Macular Inherited Retinal Dystrophies
- ATXN7-Related Cone-Rod Dystrophy: The Integrated Functional Evaluation of the Cerebellum (CERMOI) Study
- Autosomal Recessive Rod-Cone Dystrophy with Mild Extra-Ocular Manifestations Due to a Splice-Affecting Variant in BBS9
- Bardet-Biedl syndrome: A clinical overview focusing on diagnosis, outcomes and best-practice management
- Bilateral helicoid peri-papillary sub-retinal fibrosis due to a biallelic <em>NR2E3</em> mutation: Describing variable expressivity of a mutation
- Cholesterol regulates plasma membrane bending by prominin-family proteins
- Chromatic vision and structural assessment in primary congenital glaucoma
- Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy
- Clinical, Genotypic, and Imaging Characterization of the Spectrum of ABCA4 Retinopathies
- Cohen Syndrome: Novel VPS13B Genetic Variants in a Male Portuguese Patient with Pigmentary Retinopathy
- Colour vision deficiency in teaching dermatology
- Comparison of Two Printed Pseudoisochromatic Tests for Color Vision Assessment
- Contributed Session III: AAV-mediated gene therapy for PDE6C achromatopsia: Progress and challenges
- Dentofacial manifestations in a child with Jalili syndrome
- Diagnostic Challenges in <em>ABCA4</em>-Associated Retinal Degeneration: One Gene, Many Phenotypes
- Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
- Diverse retinal-kidney phenotypes associated with <em>NPHP1</em> homozygous whole-gene deletions in patients with kidney failure
- Double Hyperautofluorescence Rings as a Sign of CFAP410-related Retinopathy
- Empirical tests of the effectiveness of EnChroma multi-notch filters for enhancing color vision in deuteranomaly
- EQ-5D-5L health utility scores in Australian adults with inherited retinal diseases: A cross-sectional survey
- Excessive tubulin glutamylation leads to progressive cone-rod dystrophy and loss of outer segment integrity
- Four different gene-related cone-rod dystrophy: clinical and genetic findings in six Chinese families with diverse modes of inheritance
- Frequency and distribution of ophthalmic surgical procedures among patients with inherited retinal diseases
- Functional vision disorder: a review of diagnosis, management and costs
- Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion
- Genetics of Retinitis Pigmentosa and Other Hereditary Retinal Disorders in Western Switzerland
- Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis
- Germline knockout of <em>Nr2e3</em> protects photoreceptors in three distinct mouse models of retinal degeneration
- GNB1-Related Rod-Cone Dystrophy: A Case Report
- Heimler syndrome with a complaint of blurred vision caused by compound heterozygous variants in <em>PEX1</em>
- Heterogeneity in the progression of retinal pathologies in mice harboring patient mimicking Impg2 mutations
- HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis
- Highly efficient capture approach for the identification of diverse inherited retinal disorders
- Identifying causes of vision loss and assistive technology needs among patients attending rehabilitation clinic of a tertiary care center in North India
- IQCB1 (NPHP5)-retinopathy: Clinical and Genetic Characterization and Natural History
- Laurence-Moon-Bardet Biedl Syndrome With Cholelithiasis
- Longitudinal Assessment of OCT-Based Measures of Foveal Cone Structure in Achromatopsia
- Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration
- Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in <em>ABCA4</em>-Related Retinal Dystrophy in an Eastern European Population
- Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population
- Mechanisms of cone sensitivity loss in retinitis pigmentosa
- Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites
- Multimodal imaging of USH2A rod-cone dystrophy: Case report
- Multimodal Ophthalmic Imaging in Spinocerebellar Ataxia Type 7
- Mutational Profile and Retinal Phenotypes of PCARE-Related Cone-Rod Dystrophies in a Mexican Cohort
- Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction
- Nationwide epidemiologic survey on incidence of macular dystrophy in Japan
- Natural history and biomarkers of KCNV2-associated retinopathy
- Novel <em>ATF6</em> homozygous variant in a Chinese patient with achromatopsia
- Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss
- Novel pathogenic variants in Tubulin Tyrosine Like 5 (<em>TTLL5)</em> associated with cone-dominant retinal dystrophies and an abnormal optical coherence tomography phenotype
- Novel pathogenic variants in Tubulin Tyrosine Like 5 (TTLL5) associated with cone-dominant retinal dystrophies and an abnormal optical coherence tomography phenotype
- Pathogenicity and functional analysis of CFAP410 mutations causing cone-rod dystrophy with macular staphyloma
- Peripapillary vessel density in eyes with cone-rod dystrophy
- Phenotypic and Genetic Alterations in Adult-Onset Cone and Cone-Rod Dystrophy
- 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 syndro
- Poster Session II: Non-degenerating double cone opsin knockout mouse model of blue cone monochromacy
- Poster Session II: XR-based personalized active aid for color deficient observers
- Predicted effectiveness of EnChroma multi-notch filters for enhancing color perception in anomalous trichromats
- Prevalence and genotypic frequency of color vision defects among primary schoolchildren in Adama Town, Eastern Ethiopia
- Prominin 1 and Tweety Homology 1 both induce extracellular vesicle formation
- Protein modeling and in silico analysis to assess pathogenicity of <em>ABCA4</em> variants in patients with inherited retinal disease
- Pseudovitelliform maculopathy associated with hereditary hemochromatosis
- Recombinant protein delivery enables modulation of the phototransduction cascade in mouse retina
- Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration
- Research progress of RP1L1 gene in disease
- RiTe conjugate mediated corneal collagen crosslinking, a novel therapeutic intervention for keratoconus - in vitro and in vivo study
- RP1 Dominant p.Ser740* Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod-Cone Dystrophy: Potential Founder Effect in Western Sicily
- RTN4IP1-associated non-syndromic optic neuropathy and rod-cone dystrophy
- Should Colour Vision Deficiency be a Factor for Considering Admission to Nursing Education Programs?
- Shwachman-Diamond syndrome associated with rod-cone dystrophy
- Sstr2 Defines the Cone Differentiation-Competent Late-Stage Retinal Progenitor Cells in the Developing Mouse Retina
- Statistical Evaluation of ERG Responses: A New Method to Validate Cycle-by-Cycle Recordings in Advanced Retinal Degenerations
- Structural and functional characterization of an individual with the M285R <em>KCNV2</em> hypomorphic allele
- Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation
- Structure-function correlation of retinal photoreceptors in PRPH2-associated central areolar choroidal dystrophy patients assessed by high-resolution scanning laser imaging and microperimetry
- Subluxated cataractous lens and high myopia: An uncommon association in an achondroplasia child
- Suspected case of benign familial fleck retina with functional loss
- The construction of genetics teaching resources related to colour blindness and their application in genetics teaching
- Towards a Long-Read Sequencing Approach for the Molecular Diagnosis of RPGR<sup>ORF15</sup> Genetic Variants
- Understanding the relationship between pachychoroid spectrum disorders and retinitis pigmentosa: A review of the evidence
- Unique phenotypic-genotypic correlation in Saudi patients with <em>ALMS1</em> mutations
- Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy
- Whole genome sequencing for inherited retinal diseases in the Korean National Project of Bio Big Data
- X-linked cone dystrophy with an uncommon tapetal-like sheen caused by a novel RPGR variant