You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal recessive limb-girdle muscular dystrophy type 2G, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal recessive limb-girdle muscular dystrophy type 2G hub →Autosomal recessive limb-girdle muscular dystrophy type 2G is a rare condition. Also known as Autosomal recessive limb-girdle muscular dystrophy type 2G, LGMD due to telethonin deficiency, LGMD type 2G, LGMD2G, Limb-girdle muscular dystrophy due to telethonin deficiency, Limb-girdle muscular dystrophy type 2G, Telethonin-related LGMD R7. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive limb-girdle muscular dystrophy type 2G so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:34514 · OMIM 601954 · ICD-10 G71.0 · GARD 0010471
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive limb-girdle muscular dystrophy type 2G, 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 Autosomal recessive limb-girdle muscular dystrophy type 2G, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive limb-girdle muscular dystrophy type 2G from ClinicalTrials.gov on the hub.