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 2D, 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 2D hub →Autosomal recessive limb-girdle muscular dystrophy type 2D is a rare condition. Also known as Alpha-sarcoglycan-related LGMD R3, Alpha-sarcoglycanopathy, Autosomal recessive limb-girdle muscular dystrophy type 2D, LGMD due to alpha-sarcoglycan deficiency, LGMD type 2D, LGMD2D, Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency, Limb-girdle muscular dystrophy type 2D. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive limb-girdle muscular dystrophy type 2D so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:62 · OMIM 608099 · ICD-10 G71.0 · GARD 0000438
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive limb-girdle muscular dystrophy type 2D, 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 2D, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive limb-girdle muscular dystrophy type 2D from ClinicalTrials.gov on the hub.