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familial idiopathic torsion dystonia - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

familial idiopathic torsion dystonia

MONDO:0044816

Also known as:familial Idiopathic dystoniahereditary idiopathic torsion dystoniaidiopathic familial dystonia

Overview

An instance of idiopathic torsion dystonia that is caused by an inherited modification of the individual's genome.

Diagnosis

Biomarker and diagnostic research for familial idiopathic torsion dystonia 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 idiopathic torsion dystonia.

110 publications have been identified in PubMed for familial idiopathic torsion dystonia. Research spans Review / Meta-Analysis (25%), Basic Science / Preclinical (24%), and Clinical Trial Publication (15%).

Research Type	Count	% of Total
Research summaries	28	25%

Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 4:38 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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familial idiopathic torsion dystonia

Overview

Diagnosis

Research Landscape

Medical References

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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