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facial arteriovenous malformation - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

facial arteriovenous malformation

MONDO:0015500

Overview

Facial arteriovenous malformation is a rare vascular anomaly characterized by abnormal communication between arteries and veins, bypassing the capillary bed, located in the facial area. Lesions may be asymptomatic or may manifest with pain, ulceration, pulsation, tinnitus, minor bleeding or potentially life-threatening hemorrhage, blurred vision, impaired hearing, headache, paresthesia, enlargement of facial bones with intraosseous lesions, intraosseous hemangiomas, and speech, breathing and swallowing difficulties, as well as neuropathy.

ResearchLimited published research (4 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 facial arteriovenous malformation.

4 publications have been identified in PubMed for facial arteriovenous malformation. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (25%), and Clinical Trial Publication (25%).

Recent Publications

Boccara O (2025). [PMID: 39885577](https://pubmed.ncbi.nlm.nih.gov/39885577/). *Orphanet journal of rare diseases*. [Review / Meta-Analysis]
Pedun B (2025). [PMID: 39876926](https://pubmed.ncbi.nlm.nih.gov/39876926/). *Clinical case reports*. [Case Report / Case Series]
Nair V (2024). [PMID: 39042006](https://pubmed.ncbi.nlm.nih.gov/39042006/). *Neurology India*. [Case Report / Case Series]
Chaulagain R (2024). [PMID: 38686263](https://pubmed.ncbi.nlm.nih.gov/38686263/). *Cureus*. [Clinical Trial Publication]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 3:20 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:156230

GARD

Genetic and Rare Diseases Info Center

GARD:12663

Questions for Your Care Team

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facial arteriovenous malformation

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team