You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Merosin deficient congenital muscular dystrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Merosin deficient congenital muscular dystrophy hub →Merosin deficient congenital muscular dystrophy is a rare condition. Also known as CMD1A, Congenital muscular dystrophy due to laminin alpha2 deficiency, Congenital muscular dystrophy type 1A, MDC1A, Merosin-negative congenital muscular dystrophy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Merosin deficient congenital muscular dystrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:258 · OMIM 607855 · ICD-10 G71.2 · GARD 0003843
Start by learning the basics from an authoritative source, find a specialist or center that sees Merosin deficient congenital muscular dystrophy, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Merosin deficient congenital muscular dystrophy, filtered to your area.
Tomeko shows live, recruiting studies for Merosin deficient congenital muscular dystrophy from ClinicalTrials.gov on the hub.