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

Rare Disease

frontonasal arteriovenous malformation

MONDO:0015400

Overview

Frontonasal arteriovenous malformation is a rare vascular anomaly characterized by abnormal communication between arteries and veins, bypassing the capillary bed, located in the frontonasal area. It may present with intermittent nasal bleeding, blurred vision, pustule formation and/or disfigurement. Overlying skin may be of normal appearance or may manifest a red, pulsatile mass with local rise of temperature. Other features may include pain, ulceration, excessive growth and/or congestive heart failure.

ResearchLimited published research (2 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 frontonasal arteriovenous malformation.

2 publications have been identified in PubMed for frontonasal arteriovenous malformation. Research spans Review / Meta-Analysis (100%).

Recent Publications

Boccara O (2025). [PMID: 39885577](https://pubmed.ncbi.nlm.nih.gov/39885577/). *Orphanet J Rare Dis*. [Review / Meta-Analysis]
Gama SM (2025). [PMID: 40562378](https://pubmed.ncbi.nlm.nih.gov/40562378/). *Arq Neuropsiquiatr*. [Review / Meta-Analysis]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:55 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:141168

GARD

Genetic and Rare Diseases Info Center

GARD:19955

Questions for Your Care Team

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frontonasal 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