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familial recurrent peripheral facial palsy - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial recurrent peripheral facial palsy

MONDO:0007592

Also known as:familial recurrent Bell palsyfacial palsy, familial recurrent peripheral

Overview

GeneticsAutosomal dominant

ResearchLimited published research (6 articles)

Clinical Presentation

Features include: Facial palsy.

Organ System	Phenotype Count	Example Features
Head and neck	1	Facial palsy

Explore clinical features

Diagnosis

Biomarker and diagnostic research for familial recurrent peripheral facial palsy has been reported in the published literature.

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 recurrent peripheral facial palsy.

7 publications have been identified in PubMed for familial recurrent peripheral facial palsy. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (33%), and Diagnostic / Biomarker (17%).

Recent Publications

de Andrade HR (2025). [PMID: 40096713](https://pubmed.ncbi.nlm.nih.gov/40096713/). *Journal of neurosurgery. Case lessons*. [Case Report / Case Series]
Inzirillo K (2025). [PMID: 41179070](https://pubmed.ncbi.nlm.nih.gov/41179070/). *Cureus*. [Case Report / Case Series]
Al Jaber MY (2025). [PMID: 40330218](https://pubmed.ncbi.nlm.nih.gov/40330218/). *Risk management and healthcare policy*. [Diagnostic / Biomarker]
Alqahtani SY (2024). [PMID: 39587480](https://pubmed.ncbi.nlm.nih.gov/39587480/). *Ear, nose, & throat journal*. [Epidemiology / Natural History]
Melhem AM (2024). [PMID: 38810236](https://pubmed.ncbi.nlm.nih.gov/38810236/). *The Journal of craniofacial surgery*. [Epidemiology / Natural History]

Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 12:47 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:134200

Orphanet

European rare disease database

Orphanet:2809

GARD

Genetic and Rare Diseases Info Center

GARD:16609

Questions for Your Care Team

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familial recurrent peripheral facial palsy

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team