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euryblepharon - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

euryblepharon

MONDO:0020464

Overview

Euryblepharon is a rare congenital eyelid anomaly of unknown etiology characterized by the bilateral horizontal enlargement of the palpebral fissure with vertically shortened eyelids, lateral canthus malpositioning and lateral ectropion. It may be isolated or associated with other ocular anomalies (e.g. strabismus or telecanthus) or systemic anomalies (e.g. blepharo-cheilo-odontic syndrome). In severe cases, it may result in lagophthalmos and exposure keratopathy, requiring surgical treatment.

ResearchLimited published research (7 articles)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for euryblepharon.

7 publications have been identified in PubMed for euryblepharon. Research spans Case Report / Case Series (43%), Review / Meta-Analysis (29%), and Other (14%).

Recent Publications

Letourneau AR (2026). [PMID: 41795230](https://pubmed.ncbi.nlm.nih.gov/41795230/). *Vet Ophthalmol*. [Case Report / Case Series]
Altahan FA (2025). [PMID: 41184213](https://pubmed.ncbi.nlm.nih.gov/41184213/). *Ophthalmic Genet*. [Review / Meta-Analysis]
Sidhu AS (2025). [PMID: 39442179](https://pubmed.ncbi.nlm.nih.gov/39442179/). *Orbit*. [Case Report / Case Series]
Cardoso RV (2025). [PMID: 39277811](https://pubmed.ncbi.nlm.nih.gov/39277811/). *Vet Ophthalmol*. [Other]
Panneerselvam S (2025). [PMID: 39718141](https://pubmed.ncbi.nlm.nih.gov/39718141/). *Ophthalmic Plast Reconstr Surg*. [Review / Meta-Analysis]
Samia-Aly E (2025). [PMID: 39704292](https://pubmed.ncbi.nlm.nih.gov/39704292/). *Ophthalmic Plast Reconstr Surg*. [Clinical Trial Publication]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 2:51 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:99172

GARD

Genetic and Rare Diseases Info Center

GARD:19674

Questions for Your Care Team

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euryblepharon

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team