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

Comprehensive Analysis of Congenital Aniridia and Differential Diagnoses: Genetic Insights and Clinical Manifestations

26 Mar 2025

Abstract excerpt

INTRODUCTION: Congenital aniridia (CA) is a severe and complex disorder involving the entire eye, primarily characterized by iris anomalies alongside other clinical features that pose significant risks to vision. This study seeks to offer a comprehensive overview of CA by detailing its clinical presentations, genetic underpinnings, associated phenotypes, and differential diagnoses. Additionally, it proposes a...

Read the complete abstract on PubMed

Topics

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

Share to Developmental Biology and Gene Regulation
Share to Intraocular Surgery and Lenses
Share to Retinal Development and Disorders

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

Source

Identifiers

PMID: 40138169
DOI: 10.1007/s40123-025-01122-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 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

Comprehensive Analysis of Congenital Aniridia and Differential Diagnoses: Genetic Insights and Clinical ManifestationsPMID 40138169Read ↗

Genetics and epidemiology of aniridia: Updated guidelines for genetic study.Semantic proximity Read ↗

Clinical and molecular aspects of congenital aniridia - A review of current concepts.Semantic proximity Read ↗

Congenital aniridia beyond black eyes: From phenotype and novel genetic mechanisms to innovative therapeutic approaches.Semantic proximity Read ↗

Congenital aniridia: etiology, manifestations and managementSemantic proximity Read ↗

Congenital Aniridia: Clinic, Genetics, Therapeutics, and PrognosisSemantic proximity Read ↗

Congenital aniridia: European COST action ANIRIDIA-NET guidelines for diagnosis, management and care.Semantic proximity Read ↗

Aniridia.Semantic proximity Read ↗

The genetics of aniridia - simple things become complicated.Semantic proximity Read ↗

[Clinical features and genetic analysis for PAX6-associated ocular diseases].Semantic proximity Read ↗

New horizons in aniridia management: Clinical insights and therapeutic advancesSemantic proximity Read ↗

Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms.Semantic proximity Read ↗

Clinical and molecular aspects of aniridia.Semantic proximity Read ↗

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