Just diagnosed with Congenital muscular dystrophy?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital muscular dystrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Congenital muscular dystrophy hub →Overview
Congenital muscular dystrophy is a rare condition. Also known as CMD, MDC. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital muscular dystrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:97242 · GARD 0009138
Find care for Congenital muscular dystrophy
Authoritative references for Congenital muscular dystrophy
Research & market landscape for Congenital muscular dystrophy
Following Congenital muscular dystrophy for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Congenital muscular dystrophy — the real-world landscape behind the condition, in one place.
- Latest Congenital muscular dystrophy research on PubMed ↗
- Recruiting Congenital muscular dystrophy trials on ClinicalTrials.gov ↗
- Explore the Congenital muscular dystrophy research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Congenital muscular dystrophy and every rare condition. See how Tomeko works with industry →
Common questions
What is Congenital muscular dystrophy?
Congenital muscular dystrophy is a rare condition. Also known as CMD, MDC. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Congenital muscular dystrophy together in one place.
What are the symptoms of Congenital muscular dystrophy?
Symptoms of Congenital muscular dystrophy vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Congenital muscular dystrophy.
How is Congenital muscular dystrophy treated?
Treatment for Congenital muscular dystrophy depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Congenital muscular dystrophy, and review current options with them.
What causes Congenital muscular dystrophy — is it genetic?
The cause and inheritance of Congenital muscular dystrophy are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Congenital muscular dystrophy can explain what it means for you and your family.
I was just diagnosed with Congenital muscular dystrophy — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital muscular dystrophy, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Congenital muscular dystrophy?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Congenital muscular dystrophy, filtered to your area.
Are there clinical trials for Congenital muscular dystrophy?
Tomeko shows live, recruiting studies for Congenital muscular dystrophy from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Congenital multicore myopathy with external ophthalmoplegia
- Congenital muscular dystrophy 1B
- Congenital mitral valve insufficiency and/or stenosis
- Congenital muscular dystrophy caused by variation in POMGNT2
- Congenital mitral valve agenesis
- Congenital muscular dystrophy due to integrin alpha-7 deficiency
- Congenital mitral stenosis
- Congenital muscular dystrophy due to LMNA mutation