You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary myopathy with lactic acidosis due to ISCU deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hereditary myopathy with lactic acidosis due to ISCU deficiency hub →Hereditary myopathy with lactic acidosis due to ISCU deficiency is a rare condition. Also known as ISCU-related myopathy, Myopathy due to succinate dehydrogenase and aconitase deficiency, Myopathy with exercise intolerance, Swedish type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary myopathy with lactic acidosis due to ISCU deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:43115 · OMIM 255125 · ICD-10 G71.3 · GARD 0016643
Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary myopathy with lactic acidosis due to ISCU deficiency, 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 Hereditary myopathy with lactic acidosis due to ISCU deficiency, filtered to your area.
Tomeko shows live, recruiting studies for Hereditary myopathy with lactic acidosis due to ISCU deficiency from ClinicalTrials.gov on the hub.