Autosomal recessive spastic paraplegia type 21

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ORPHA:101001OMIM:248900G11.4
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8Treatment centers

Where are you in your journey?

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

Also known as:

Clinical phenotype terms— hover any for plain English:

ApraxiaHP:0002186Primitive reflexHP:0002476Abnormality of peripheral nerve conductionHP:0003134Frontotemporal cerebral atrophyHP:0006892DysgraphiaHP:0010526Personality disorderHP:0012075
Orphanet ↗OMIM ↗NORD ↗

FDA & Trial Timeline

4 events
Oct 2025Screening Study for KIT D816V Mutated Mast Cell Disease in Select Populations

Blueprint Medicines Corporation

TrialRECRUITING
May 2024Budesonide as a Treatment for Functional Dyspepsia

Universitaire Ziekenhuizen KU Leuven — PHASE4

TrialRECRUITING
Jan 2024Role of Tryptase Levels in Patients With Stable Coronary Artery Disease.

University of Thessaly

TrialRECRUITING
Sep 2022Prevalence of Mast Cell Activation Syndrome in Patients With EDS With Digestive Disorders

Lille Catholic University

TrialRECRUITING

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

Treatments

No FDA-approved treatments are currently listed for Autosomal recessive spastic paraplegia type 21.

View clinical trials →

No actively recruiting trials found for Autosomal recessive spastic paraplegia type 21 at this time.

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

Search ClinicalTrials.gov ↗Join the Autosomal recessive spastic paraplegia type 21 community →

No specialists are currently listed for Autosomal recessive spastic paraplegia type 21.

View NORD Rare Disease Centers ↗Undiagnosed Disease Network ↗

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 recessive spastic paraplegia type 21.

Search all travel grants →NORD Financial Assistance ↗

Community

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Latest news about Autosomal recessive spastic paraplegia type 21

Disease timeline:

New recruiting trial: Budesonide as a Treatment for Functional Dyspepsia

A new clinical trial is recruiting patients for Autosomal recessive spastic paraplegia type 21

New recruiting trial: Screening Study for KIT D816V Mutated Mast Cell Disease in Select Populations

A new clinical trial is recruiting patients for Autosomal recessive spastic paraplegia type 21

New recruiting trial: Prevalence of Mast Cell Activation Syndrome in Patients With EDS With Digestive Disorders

A new clinical trial is recruiting patients for Autosomal recessive spastic paraplegia type 21

New recruiting trial: Role of Tryptase Levels in Patients With Stable Coronary Artery Disease.

A new clinical trial is recruiting patients for Autosomal recessive spastic paraplegia type 21

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.