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Inherited pseudoxanthoma elasticum

Just diagnosed with Inherited pseudoxanthoma elasticum?

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

Open the full Inherited pseudoxanthoma elasticum hub →

Overview

Inherited pseudoxanthoma elasticum is a rare condition. Also known as Gronblad-Strandberg-Touraine syndrome, PXE. Tomeko brings together the specialists, research, clinical trials, treatments and community for Inherited pseudoxanthoma elasticum so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:758 · OMIM 177850, 264800 · ICD-10 Q82.8 · GARD 0009643

Find care for Inherited pseudoxanthoma elasticum

Authoritative references for Inherited pseudoxanthoma elasticum

Common questions

I was just diagnosed with Inherited pseudoxanthoma elasticum — what should I do first?

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

Where can I find a specialist for Inherited pseudoxanthoma elasticum?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Inherited pseudoxanthoma elasticum, filtered to your area.

Are there clinical trials for Inherited pseudoxanthoma elasticum?

Tomeko shows live, recruiting studies for Inherited pseudoxanthoma elasticum 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