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familial multiple meningioma - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial multiple meningioma

MONDO:0016995

Overview

Familial multiple meningioma is a rare, benign neoplasm of the central nervous system characterized by the development of multiple or, rarely, solitary meningiomas in two or more blood relatives, without other apparent syndromic manifestations. Depending on the localization, growth rate and size of the tumors, patients can present with subtle, gradually worsening or abrupt and severe neurological compromise or can be completely asymptomatic.

Diagnosis

Biomarker and diagnostic research for familial multiple meningioma has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

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 familial multiple meningioma.

76 publications have been identified in PubMed for familial multiple meningioma. Research spans Review / Meta-Analysis (26%), Case Report / Case Series (26%), and Epidemiology / Natural History (19%).

Research Type	Count	% of Total
Research summaries	19	26%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 8:40 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:263662

GARD

Genetic and Rare Diseases Info Center

GARD:17260

Questions for Your Care Team

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familial multiple meningioma

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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