You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Sarcotubular myopathy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Sarcotubular myopathy hub →Sarcotubular myopathy is a rare condition. Also known as Autosomal recessive limb-girdle muscular dystrophy type 2H, LGMD due to TRIM32 deficiency, LGMD type 2H, LGMD2H, Limb-girdle muscular dystrophy due to TRIM32 deficiency, Limb-girdle muscular dystrophy type 2H, Sarcotubular myopathy, TRIM32-related LGMD R8. Tomeko brings together the specialists, research, clinical trials, treatments and community for Sarcotubular myopathy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1878 · OMIM 254110 · ICD-10 G71.0 · GARD 0003844
Start by learning the basics from an authoritative source, find a specialist or center that sees Sarcotubular myopathy, 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 Sarcotubular myopathy, filtered to your area.
Tomeko shows live, recruiting studies for Sarcotubular myopathy from ClinicalTrials.gov on the hub.