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 interactive 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
- Alexander Graham Bell Association for the Deaf and Hard of Hearing
- American Society for Deaf Children
Authoritative references for Perrault syndrome
Research & market landscape for Perrault syndrome
Following Perrault syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Perrault syndrome — the real-world landscape behind the condition, in one place.
- Latest Perrault syndrome research on PubMed ↗
- Recruiting Perrault syndrome trials on ClinicalTrials.gov ↗
- Explore the Perrault syndrome research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Perrault syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Perrault syndrome?
Perrault syndrome is a rare condition. Also known as XX gonadal dysgenesis-deafness syndrome, XX gonadal dysgenesis-hearing loss syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Perrault syndrome together in one place.
What are the symptoms of Perrault syndrome?
Symptoms of Perrault syndrome vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Perrault syndrome.
How is Perrault syndrome treated?
Treatment for Perrault syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Perrault syndrome, and review current options with them.
What causes Perrault syndrome — is it genetic?
The cause and inheritance of Perrault syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Perrault syndrome can explain what it means for you and your family.
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.
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