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Allan-Herndon-Dudley syndrome

Just diagnosed with Allan-Herndon-Dudley syndrome?

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

Open the full Allan-Herndon-Dudley syndrome hub →

Overview

Allan-Herndon-Dudley syndrome is a rare condition. Also known as AHDS, MCT8 deficiency, Monocarboxylate transporter 8 deficiency, X-linked intellectual disability-hypotonia syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Allan-Herndon-Dudley syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:59 · OMIM 300523 · ICD-10 E03.8 · GARD 0005617

Find care for Allan-Herndon-Dudley syndrome

Authoritative references for Allan-Herndon-Dudley syndrome

Common questions

I was just diagnosed with Allan-Herndon-Dudley syndrome — what should I do first?

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

Where can I find a specialist for Allan-Herndon-Dudley syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Allan-Herndon-Dudley syndrome, filtered to your area.

Are there clinical trials for Allan-Herndon-Dudley syndrome?

Tomeko shows live, recruiting studies for Allan-Herndon-Dudley syndrome 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