Autosomal dominant cerebellar ataxia type I

Last reviewed

🖨 Print for my doctorAdvocacy Hub →
ORPHA:94145
Who is this for?
Show terms as
2Specialists8Treatment centers

Where are you in your journey?

UniteRare data is sourced from FDA.gov, ClinicalTrials.gov, Orphanet, OMIM, and NORD.
Report missing data

Overview

Also known as:

Orphanet ↗NORD ↗

FDA & Trial Timeline

2 events
Jan 2021Home Based Tele-exercise for People With Chronic Neurological Impairments

Burke Medical Research Institute — NA

TrialACTIVE NOT RECRUITING
Oct 2014Cerebellar Mutism Syndrome Study

Rigshospitalet, Denmark

TrialRECRUITING

Data sourced from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Treatments

No FDA-approved treatments are currently listed for Autosomal dominant cerebellar ataxia type I.

View clinical trials →

No actively recruiting trials found for Autosomal dominant cerebellar ataxia type I at this time.

New trials open frequently. Follow this disease to get notified.

Search ClinicalTrials.gov ↗Join the Autosomal dominant cerebellar ataxia type I community →

Specialists

2 foundView all specialists →
AM
Anissa MEGZARI
Specialist
PI on 15 active trials1 Autosomal dominant cerebellar ataxia type I publication

Treatment Centers

8 centers
🏥 NORD

Baylor College of Medicine Rare Disease Center

Baylor College of Medicine

📍 Houston, TX

🏥 NORD

Stanford Medicine Rare Disease Center

Stanford Medicine

📍 Stanford, CA

🔬 UDN

NIH Clinical Center Undiagnosed Diseases Program

National Institutes of Health

📍 Bethesda, MD

🔬 UDN

UCLA UDN Clinical Site

UCLA Health

📍 Los Angeles, CA

🔬 UDN

Baylor College of Medicine UDN Clinical Site

Baylor College of Medicine

📍 Houston, TX

🔬 UDN

Harvard/MGH UDN Clinical Site

Massachusetts General Hospital

📍 Boston, MA

🏥 NORD

Mayo Clinic Center for Individualized Medicine

Mayo Clinic

📍 Rochester, MN

👤 Mayo Clinic Center for Individualized Medicine

🏥 NORD

UCLA Rare Disease Day Program

UCLA Health

📍 Los Angeles, CA

Travel Grants

No travel grants are currently matched to Autosomal dominant cerebellar ataxia type I.

Search all travel grants →NORD Financial Assistance ↗

Community

Open Autosomal dominant cerebellar ataxia type IForum →

No community posts yet. Be the first to share your experience with Autosomal dominant cerebellar ataxia type I.

Start the conversation →

Latest news about Autosomal dominant cerebellar ataxia type I

Disease timeline:

New recruiting trial: Modifiable Variables in Parkinsonism (MVP)

A new clinical trial is recruiting patients for Autosomal dominant cerebellar ataxia type I

New recruiting trial: The CurePSP Genetics Program

A new clinical trial is recruiting patients for Autosomal dominant cerebellar ataxia type I

New recruiting trial: Cerebellar Mutism Syndrome Study

A new clinical trial is recruiting patients for Autosomal dominant cerebellar ataxia type I

Caregiver Resources

NORD Caregiver Resources

Support, advocacy, and financial assistance for caregivers of rare disease patients.

Mental Health Support

Rare disease caregiving can be isolating. Connect with counseling and peer support.

Family & Caregiver Grants

Financial assistance programs specifically for caregivers of rare disease patients.

Social Security Disability

Learn how rare disease patients may qualify for SSDI/SSI benefits.

Common questions about Autosomal dominant cerebellar ataxia type I

Which specialists treat Autosomal dominant cerebellar ataxia type I?

2 specialists and care centers treating Autosomal dominant cerebellar ataxia type I are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.