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Article

Underlying Disease in Atypical Retinopathy of Prematurity.

American journal of ophthalmology - 1 Jun 2025

Cruz Natasha F S DA, Hudson Julia L, Sengillo Jesse D, Shah Serena M, Lopez-Font Francisco, Negron Catherin I, Farah Michel E, Berrocal Audina M

Abstract excerpt

BACKGROUND AND OBJECTIVE: Retinopathy of prematurity (ROP), familial exudative vitreoretinopathy (FEVR), and telomere biology disorders (TBD) are classified as distinct diseases. However, emerging genetic research and evidence on multimodal imaging suggest a spectrum along which ROP may overlap with FEVR or TBD. DESIGN: Retrospective case series. METHODS: This was an institutional review board-approved,...

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Source

Identifiers

PMID: 40010420
DOI: 10.1016/j.ajo.2025.02.026

Genes

CTC1
FZD4
LRP5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

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Underlying Disease in Atypical Retinopathy of Prematurity.PMID 40010420Read ↗

The Genetics and Clinical Variables of Retinopathy of Prematurity: A Matched Case Control StudySemantic proximity Read ↗

Genetic susceptibility to advanced retinopathy of prematurity (ROP).Semantic proximity Read ↗

Comparisons of Genetic and Clinical Findings in Patients with Syndromic to Non-Syndromic Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

Genetic Characteristics and Clinical Manifestations of Foveal Hypoplasia in Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

Reaching a FEVR Pitch: A Case Series of Familial Exudative Vitreoretinopathy in Northern Ireland.Semantic proximity Read ↗

Frizzled-4 Variations Associated with Retinopathy and Intrauterine Growth Retardation: A Potential Marker for Prematurity and Retinopathy.Semantic proximity Read ↗

LONG-TERM CLINICAL OUTCOMES AND GENOTYPE-PHENOTYPE CORRELATION IN FAMILIAL EXUDATIVE VITREORETINOPATHY IN A TERTIARY REFERRAL CENTER.Semantic proximity Read ↗

A novel variant in the FZD4 gene leading to familial exudative vitreoretinopathy: A case report and literature review.Semantic proximity Read ↗

Genetics in Retinal Diseases.Semantic proximity Read ↗

Genetics of the retina.Semantic proximity Read ↗

Mutation spectrum in a cohort with familial exudative vitreoretinopathy.Semantic proximity Read ↗

Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 Involvement.Semantic proximity Read ↗

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