Overview
Treatments
No FDA-approved treatments are currently listed for Congenital muscular dystrophy type 1B.
View clinical trials →Clinical Trials
View all trials with filters →No actively recruiting trials found for Congenital muscular dystrophy type 1B at this time.
New trials open frequently. Follow this disease to get notified.
Rare Disease Specialist
Treatment Centers
8 centersBaylor College of Medicine Rare Disease Center ↗
Baylor College of Medicine
📍 Houston, TX
🏥 NORDStanford Medicine Rare Disease Center ↗
Stanford Medicine
📍 Stanford, CA
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
🔬 UDNUCLA UDN Clinical Site ↗
UCLA Health
📍 Los Angeles, CA
🔬 UDNBaylor College of Medicine UDN Clinical Site ↗
Baylor College of Medicine
📍 Houston, TX
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDMayo Clinic Center for Individualized Medicine ↗
Mayo Clinic
📍 Rochester, MN
👤 Mayo Clinic Center for Individualized Medicine
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
Travel Grants
No travel grants are currently matched to Congenital muscular dystrophy type 1B.
Community
No community posts yet. Be the first to share your experience with Congenital muscular dystrophy type 1B.
Start the conversation →Latest news about Congenital muscular dystrophy type 1B
Disease timeline:
New recruiting trial: Mayo AVC Registry and Biobank
A new clinical trial is recruiting patients for Congenital muscular dystrophy type 1B
New recruiting trial: A Study of the Efficacy and Safety of Danicamtiv in Participants With Symptomatic Genetic and Familial Dilated Cardiomyopathy
A new clinical trial is recruiting patients for Congenital muscular dystrophy type 1B
New recruiting trial: A Study to Evaluate Del-brax (Also Referred to as AOC 1020) in Participants With FSHD
A new clinical trial is recruiting patients for Congenital muscular dystrophy type 1B
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 Congenital muscular dystrophy type 1B
Which specialists treat Congenital muscular dystrophy type 1B?
2 specialists and care centers treating Congenital muscular dystrophy type 1B are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.