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epilepsy with auditory features (EAF) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

epilepsy with auditory features

MONDO:0800496

Also known as:EAF

Overview

A variable-age onset focal epilepsy syndrome with characteristic focal aware sensory auditory seizures. Seizures often produce such mild symptoms that they are not diagnosed. There are no implications expected for development or learning and seizures are typically infrequent and well controlled. EAF may occur as a familial syndrome, familial EAF (FEAF, previous known as autosomal dominant lateral temporal lobe epilepsy or autosomal dominant partial epilepsy with auditory features). Inheritance may be autosomal dominant (ADEAF), with incomplete penetrance.

ResearchLimited published research (5 articles)

Diagnosis

Biomarker and diagnostic research for epilepsy with auditory features 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 epilepsy with auditory features.

5 publications have been identified in PubMed for epilepsy with auditory features. Research spans Gene Therapy / Novel Therapeutics (60%), Diagnostic / Biomarker (20%), and Review / Meta-Analysis (20%).

Recent Publications

Salman B (2026). [PMID: 41777496](https://pubmed.ncbi.nlm.nih.gov/41777496/). *Noro psikiyatri arsivi*. [Review / Meta-Analysis]
Zhang F (2025). [PMID: 40670805](https://pubmed.ncbi.nlm.nih.gov/40670805/). *Interdisciplinary sciences, computational life sciences*. [Diagnostic / Biomarker]
Hirano Y (2025). [PMID: 40455867](https://pubmed.ncbi.nlm.nih.gov/40455867/). *Brain : a journal of neurology*. [Gene Therapy / Novel Therapeutics]
Talarico M (2024). [PMID: 39796146](https://pubmed.ncbi.nlm.nih.gov/39796146/). *International journal of molecular sciences*. [Gene Therapy / Novel Therapeutics]
Bonanni P (2024). [PMID: 38654463](https://pubmed.ncbi.nlm.nih.gov/38654463/). *Epilepsia open*. [Gene Therapy / Novel Therapeutics]

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 1:53 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

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epilepsy with auditory features

Overview

Diagnosis

Research Landscape

Recent Publications

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team