You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Adult-onset proximal spinal muscular atrophy, autosomal dominant, look for clinical trials, and connect with others living with it — all in one place.
Open the full Adult-onset proximal spinal muscular atrophy, autosomal dominant hub →Adult-onset proximal spinal muscular atrophy, autosomal dominant is a rare condition. Also known as Autosomal dominant adult-onset proximal SMA, Autosomal dominant late-onset spinal muscular atrophy, Finkel type, Finkel disease, SMAFK. Tomeko brings together the specialists, research, clinical trials, treatments and community for Adult-onset proximal spinal muscular atrophy, autosomal dominant so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:209335 · OMIM 182980 · ICD-10 G12.1 · GARD 0017102
Start by learning the basics from an authoritative source, find a specialist or center that sees Adult-onset proximal spinal muscular atrophy, autosomal dominant, 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 Adult-onset proximal spinal muscular atrophy, autosomal dominant, filtered to your area.
Tomeko shows live, recruiting studies for Adult-onset proximal spinal muscular atrophy, autosomal dominant from ClinicalTrials.gov on the hub.