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epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features

MONDO:0859390

Overview

Diagnosis

Biomarker and diagnostic research for epilepsy, X-linked, with or without impaired intellectual development and dysmorphic 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, X-linked, with or without impaired intellectual development and dysmorphic features.

214 publications have been identified in PubMed for epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features. Research spans Case Report / Case Series (37%), Basic Science / Preclinical (32%), and Epidemiology / Natural History (12%).

Research Type	Count	% of Total
Patient case studies	80

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 11:55 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

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epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features

Overview

Diagnosis

Research Landscape

Medical References

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications