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Scapuloperoneal spinal muscular atrophy

Just diagnosed with Scapuloperoneal spinal muscular atrophy?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Scapuloperoneal spinal muscular atrophy, look for clinical trials, and connect with others living with it — all in one place.

Open the full Scapuloperoneal spinal muscular atrophy hub →

Overview

Scapuloperoneal spinal muscular atrophy is a rare condition. Also known as Neurogenic scapuloperoneal amyotrophy, New England type, SPSMA, Scapuloperoneal neuronopathy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Scapuloperoneal spinal muscular atrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:431255 · OMIM 181405 · ICD-10 G12.1 · GARD 0010314

Find care for Scapuloperoneal spinal muscular atrophy

Authoritative references for Scapuloperoneal spinal muscular atrophy

Common questions

I was just diagnosed with Scapuloperoneal spinal muscular atrophy — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Scapuloperoneal spinal muscular atrophy, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Scapuloperoneal spinal muscular atrophy?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Scapuloperoneal spinal muscular atrophy, filtered to your area.

Are there clinical trials for Scapuloperoneal spinal muscular atrophy?

Tomeko shows live, recruiting studies for Scapuloperoneal spinal muscular atrophy from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com