autosomal dominant cerebellar ataxia type IV | Kisho | Kisho

autosomal dominant cerebellar ataxia type IV

Rare Disease

MONDO:0019794

Also known as:

ADCA4ADCAIVautosomal dominant cerebellar ataxia type 4

Genes

Clinical Trials

1 active

Newborn Screening

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Patient Groups

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Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

How we create this content →

Feb 7, 2026

Find Clinical TrialsTrials

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

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View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Overview

autosomal dominant cerebellar ataxia type IV is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

The condition is also known by several synonyms including ADCA4 and ADCAIV. Currently, there are no known associated genes, inheritance patterns, or documented symptoms. There are no orphan drug designations under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to understand potential inheritance patterns. Connecting with rare disease registries such as Orphanet may provide additional resources and support. Finding specialists experienced with ataxias could also be beneficial.

Quick Resources

Helpful links for rare disease information and support

GARD (Genetic and Rare Diseases Information Center)NORD (National Organization for Rare Disorders)Find a Genetic Counselor

General Questions to Consider

Questions that may be helpful when speaking with your healthcare team

•Are there specialists or centers of excellence with experience in this condition?
•Is there a patient registry I could participate in?
•Should my family members consider genetic testing?
•What clinical trials might be available for this condition?
•Are there patient advocacy groups I should connect with?

Clinical

Associated Genes

2 genes

ATXN10 ATN1

Gene data from HGNC • Click to view on NCBI Gene

Treatment

Clinical Trials

Research studies investigating treatments and therapies for this condition.

Active Trials

Total Trials

Filter trials on ClinicalTrials.gov:

View Recruiting Trials View All Trials

Data from ClinicalTrials.gov Jan 6, 2026

Support

External Resources

Orphanet

European rare disease database

Orphanet:94149

GARD

Genetic and Rare Diseases Info Center

GARD:19254

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AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.

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autosomal dominant cerebellar ataxia type IV

Patient-Friendly Information

Clinical Trials

Clinical Trials

Overview

Overview

Symptoms & Signs

Prognosis & Outlook

Quick Resources

General Questions to Consider

Clinical

Associated Genes

Treatment

Clinical Trials

Support

External Resources

Orphanet

GARD

Related Diseases

Know a Patient Advocacy Group for this condition?

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