Just diagnosed with Complete trisomy 13 syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Complete trisomy 13 syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Complete trisomy 13 syndrome hub →Overview
Complete trisomy 13 syndrome is a rare condition. Also known as Patau syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Complete trisomy 13 syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3378 · ICD-10 Q91.4, Q91.5, Q91.6 · GARD 0007341
Find care for Complete trisomy 13 syndrome
Authoritative references for Complete trisomy 13 syndrome
Research & market landscape for Complete trisomy 13 syndrome
Following Complete trisomy 13 syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Complete trisomy 13 syndrome — the real-world landscape behind the condition, in one place.
- Latest Complete trisomy 13 syndrome research on PubMed ↗
- Recruiting Complete trisomy 13 syndrome trials on ClinicalTrials.gov ↗
- Explore the Complete trisomy 13 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 Complete trisomy 13 syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Complete trisomy 13 syndrome?
Complete trisomy 13 syndrome is a rare condition. Also known as Patau syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Complete trisomy 13 syndrome together in one place.
What are the symptoms of Complete trisomy 13 syndrome?
Symptoms of Complete trisomy 13 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 Complete trisomy 13 syndrome.
How is Complete trisomy 13 syndrome treated?
Treatment for Complete trisomy 13 syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Complete trisomy 13 syndrome, and review current options with them.
What causes Complete trisomy 13 syndrome — is it genetic?
The cause and inheritance of Complete trisomy 13 syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Complete trisomy 13 syndrome can explain what it means for you and your family.
I was just diagnosed with Complete trisomy 13 syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Complete trisomy 13 syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Complete trisomy 13 syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Complete trisomy 13 syndrome, filtered to your area.
Are there clinical trials for Complete trisomy 13 syndrome?
Tomeko shows live, recruiting studies for Complete trisomy 13 syndrome from ClinicalTrials.gov on the hub.
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