You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Infantile neuroaxonal dystrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Infantile neuroaxonal dystrophy hub →Infantile neuroaxonal dystrophy is a rare condition. Also known as INAD, Infantile neuroaxonal dystrophy, Infantile PLAN, Infantile phospholipase A2-associated neurodegeneration, Seitelberger disease, PLA2G6-associated neurodegeneration, infantile-onset. Tomeko brings together the specialists, research, clinical trials, treatments and community for Infantile neuroaxonal dystrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:35069 · OMIM 256600, 610217 · ICD-10 G31.8 · GARD 0003957
Start by learning the basics from an authoritative source, find a specialist or center that sees Infantile neuroaxonal dystrophy, 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 Infantile neuroaxonal dystrophy, filtered to your area.
Tomeko shows live, recruiting studies for Infantile neuroaxonal dystrophy from ClinicalTrials.gov on the hub.