You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures hub →Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures is a rare condition. Also known as DYNC1H1-related lower extremity-predominant autosomal dominant proximal spinal muscular atrophy, SMALED1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:209341 · OMIM 158600 · ICD-10 G12.1 · GARD 0013519
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures, 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 Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures from ClinicalTrials.gov on the hub.