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Hereditary spastic paraplegia 3A

Just diagnosed with Hereditary spastic paraplegia 3A?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hereditary spastic paraplegia 3A, look for clinical trials, and connect with others living with it — all in one place.

Open the full Hereditary spastic paraplegia 3A hub →

Overview

Hereditary spastic paraplegia 3A is a rare condition. Also known as Autosomal dominant spastic paraplegia type 3A, SPG3A, Strümpell disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hereditary spastic paraplegia 3A so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:100984 · OMIM 182600 · ICD-10 G11.4 · GARD 0005041

Find care for Hereditary spastic paraplegia 3A

Authoritative references for Hereditary spastic paraplegia 3A

Common questions

I was just diagnosed with Hereditary spastic paraplegia 3A — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Hereditary spastic paraplegia 3A, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Hereditary spastic paraplegia 3A?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hereditary spastic paraplegia 3A, filtered to your area.

Are there clinical trials for Hereditary spastic paraplegia 3A?

Tomeko shows live, recruiting studies for Hereditary spastic paraplegia 3A 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