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 2Y, 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 2Y hub →Autosomal recessive limb-girdle muscular dystrophy type 2Y is a rare condition. Also known as Autosomal recessive limb-girdle muscular dystrophy type 2Y, Autosomal recessive muscular dystrophy due to LAP1B deficiency, Autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency, LGMD type 2Y, LGMD2Y, Muscular dystrophy with progressive weakness, distal contractures and rigid spine, TOR1AIP1-related LGMD. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal recessive limb-girdle muscular dystrophy type 2Y so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:424261 · OMIM 617072 · ICD-10 G71.0 · GARD 0017708
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal recessive limb-girdle muscular dystrophy type 2Y, 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 2Y, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal recessive limb-girdle muscular dystrophy type 2Y from ClinicalTrials.gov on the hub.