Just diagnosed with Pallister-Killian syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Pallister-Killian syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Pallister-Killian syndrome hub →Overview
Pallister-Killian syndrome is a rare condition. Also known as Isochromosome 12p mosaicism, Isochromosome 12p syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pallister-Killian syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:884 · OMIM 601803 · ICD-10 Q99.8 · GARD 0008421
Find care for Pallister-Killian syndrome
Authoritative references for Pallister-Killian syndrome
Research & market landscape for Pallister-Killian syndrome
Following Pallister-Killian syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Pallister-Killian syndrome — the real-world landscape behind the condition, in one place.
- Latest Pallister-Killian syndrome research on PubMed ↗
- Recruiting Pallister-Killian syndrome trials on ClinicalTrials.gov ↗
- Explore the Pallister-Killian 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 Pallister-Killian syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Pallister-Killian syndrome?
Pallister-Killian syndrome is a rare condition. Also known as Isochromosome 12p mosaicism, Isochromosome 12p syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Pallister-Killian syndrome together in one place.
What are the symptoms of Pallister-Killian syndrome?
Symptoms of Pallister-Killian 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 Pallister-Killian syndrome.
How is Pallister-Killian syndrome treated?
Treatment for Pallister-Killian syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Pallister-Killian syndrome, and review current options with them.
What causes Pallister-Killian syndrome — is it genetic?
The cause and inheritance of Pallister-Killian syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Pallister-Killian syndrome can explain what it means for you and your family.
I was just diagnosed with Pallister-Killian syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Pallister-Killian syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Pallister-Killian syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Pallister-Killian syndrome, filtered to your area.
Are there clinical trials for Pallister-Killian syndrome?
Tomeko shows live, recruiting studies for Pallister-Killian syndrome from ClinicalTrials.gov on the hub.
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