You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Werdnig-Hoffmann disease, look for clinical trials, and connect with others living with it — all in one place.
Open the full Werdnig-Hoffmann disease hub →Werdnig-Hoffmann disease is a rare condition. Also known as Infantile spinal muscular atrophy, Infantile-onset spinal muscular atrophy, SMA type 1, SMA type I, SMA-I, SMA1, Werdnig-Hoffmann disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Werdnig-Hoffmann disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:83330 · OMIM 253300 · ICD-10 G12.0 · GARD 0007883
Start by learning the basics from an authoritative source, find a specialist or center that sees Werdnig-Hoffmann disease, 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 Werdnig-Hoffmann disease, filtered to your area.
Tomeko shows live, recruiting studies for Werdnig-Hoffmann disease from ClinicalTrials.gov on the hub.