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Perrault syndrome

Just diagnosed with Perrault syndrome?

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

Open the full Perrault syndrome hub →

Overview

Perrault syndrome is a rare condition. Also known as XX gonadal dysgenesis-deafness syndrome, XX gonadal dysgenesis-hearing loss syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Perrault syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:2855 · OMIM 233400, 614129, 614926 · ICD-10 Q87.8 · GARD 0002542

Find care for Perrault syndrome

Patient organizations for Perrault syndrome

Authoritative references for Perrault syndrome

Common questions

I was just diagnosed with Perrault syndrome — what should I do first?

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

Where can I find a specialist for Perrault syndrome?

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

Are there clinical trials for Perrault syndrome?

Tomeko shows live, recruiting studies for Perrault 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