You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Infantile-onset X-linked spinal muscular atrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Infantile-onset X-linked spinal muscular atrophy hub →Infantile-onset X-linked spinal muscular atrophy is a rare condition. Also known as SMAX2, Spinal muscular atrophy with arthrogryposis, X-linked distal arthrogryposis multiplex congenita, X-linked spinal muscular atrophy type 2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Infantile-onset X-linked spinal muscular atrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1145 · OMIM 301830 · ICD-10 G12.1 · GARD 0008521
Start by learning the basics from an authoritative source, find a specialist or center that sees Infantile-onset X-linked spinal muscular atrophy, 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-onset X-linked spinal muscular atrophy, filtered to your area.
Tomeko shows live, recruiting studies for Infantile-onset X-linked spinal muscular atrophy from ClinicalTrials.gov on the hub.