Limited structured data is available for this condition. Information continues to be gathered as research progresses.(5 data sources · Data coverage: Limited)

Overview

autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Symptoms & Signs

Currently, there are no known synonyms or documented associated genes for this syndrome. There is also regarding inheritance patterns, prevalence, or specific symptoms. Additionally, there are no orphan drug designations under investigation for this condition.

Prognosis & Outlook

Patients and caregivers are encouraged to seek genetic counseling to better understand potential hereditary implications. Connecting with rare disease registries, such as those provided by NORD or Orphanet, may offer additional resources and support. Finding specialists experienced with similar conditions can 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

3 genes

WWOX RUBCN TDP2

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 7, 2026

Support

External Resources

Orphanet

European rare disease database

Orphanet:404481

GARD

Genetic and Rare Diseases Info Center

GARD:21719

Know a Patient Advocacy Group for this condition?

Help patients and families find support by registering your organization or suggesting a group that serves this community.

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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 recessive cerebellar ataxia - epilepsy - intellectual disability syndrome

Patient-Friendly Information

Associated Genes

Associated Genes

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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