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Pseudo-Hurler polydystrophy

Just diagnosed with Pseudo-Hurler polydystrophy?

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

Open the full Pseudo-Hurler polydystrophy hub →

Overview

Pseudo-Hurler polydystrophy is a rare condition. Also known as ML 3 alpha/beta, ML III alpha/beta, Mucolipidosis type 3 alpha/beta. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pseudo-Hurler polydystrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:423461 · OMIM 252600 · ICD-10 E77.0 · GARD 0017704

Find care for Pseudo-Hurler polydystrophy

Authoritative references for Pseudo-Hurler polydystrophy

Common questions

I was just diagnosed with Pseudo-Hurler polydystrophy — what should I do first?

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

Where can I find a specialist for Pseudo-Hurler polydystrophy?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Pseudo-Hurler polydystrophy, filtered to your area.

Are there clinical trials for Pseudo-Hurler polydystrophy?

Tomeko shows live, recruiting studies for Pseudo-Hurler polydystrophy 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