Just diagnosed with Xq12-q13.3 duplication syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Xq12-q13.3 duplication syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Xq12-q13.3 duplication syndrome hub →Overview
Xq12-q13.3 duplication syndrome is a rare condition. Also known as Dup(X)(q12-q13.3), Kaya-Prontera syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Xq12-q13.3 duplication syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:314389 · ICD-10 Q99.8 · GARD 0021369
Find care for Xq12-q13.3 duplication syndrome
Authoritative references for Xq12-q13.3 duplication syndrome
Research & market landscape for Xq12-q13.3 duplication syndrome
Following Xq12-q13.3 duplication syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Xq12-q13.3 duplication syndrome — the real-world landscape behind the condition, in one place.
- Latest Xq12-q13.3 duplication syndrome research on PubMed ↗
- Recruiting Xq12-q13.3 duplication syndrome trials on ClinicalTrials.gov ↗
- Explore the Xq12-q13.3 duplication 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 Xq12-q13.3 duplication syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Xq12-q13.3 duplication syndrome?
Xq12-q13.3 duplication syndrome is a rare condition. Also known as Dup(X)(q12-q13.3), Kaya-Prontera syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Xq12-q13.3 duplication syndrome together in one place.
What are the symptoms of Xq12-q13.3 duplication syndrome?
Symptoms of Xq12-q13.3 duplication 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 Xq12-q13.3 duplication syndrome.
How is Xq12-q13.3 duplication syndrome treated?
Treatment for Xq12-q13.3 duplication syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Xq12-q13.3 duplication syndrome, and review current options with them.
What causes Xq12-q13.3 duplication syndrome — is it genetic?
The cause and inheritance of Xq12-q13.3 duplication syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Xq12-q13.3 duplication syndrome can explain what it means for you and your family.
I was just diagnosed with Xq12-q13.3 duplication syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Xq12-q13.3 duplication syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Xq12-q13.3 duplication syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Xq12-q13.3 duplication syndrome, filtered to your area.
Are there clinical trials for Xq12-q13.3 duplication syndrome?
Tomeko shows live, recruiting studies for Xq12-q13.3 duplication syndrome from ClinicalTrials.gov on the hub.
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