You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type, look for clinical trials, and connect with others living with it — all in one place.
Open the full Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type hub →Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type is a rare condition. Also known as COX deficiency, French-Canadian type, Cytochrome C oxidase deficiency, French-Canadian type, Cytochrome oxidase deficiency, Saguenay-Lac-Saint-Jean type, Leigh syndrome, French-Canadian type, Leigh syndrome, Saguenay-Lac-Saint-Jean type, SLSJ-COX deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:70472 · OMIM 220111, 619065 · ICD-10 G31.8 · GARD 0008370
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type, 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 Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type, filtered to your area.
Tomeko shows live, recruiting studies for Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type from ClinicalTrials.gov on the hub.