Just diagnosed with Pai syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Pai syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Pai syndrome hub →Overview
Pai syndrome is a rare condition. Also known as Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Pai syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:1993 · OMIM 155145 · ICD-10 Q87.8 · GARD 0003439
Find care for Pai syndrome
Authoritative references for Pai syndrome
Research & market landscape for Pai syndrome
Following Pai syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Pai syndrome — the real-world landscape behind the condition, in one place.
- Latest Pai syndrome research on PubMed ↗
- Recruiting Pai syndrome trials on ClinicalTrials.gov ↗
- Explore the Pai 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 Pai syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Pai syndrome?
Pai syndrome is a rare condition. Also known as Median cleft of the upper lip-corpus callosum lipoma-midline facial cutaneous polyps syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Pai syndrome together in one place.
What are the symptoms of Pai syndrome?
Symptoms of Pai 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 Pai syndrome.
How is Pai syndrome treated?
Treatment for Pai syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Pai syndrome, and review current options with them.
What causes Pai syndrome — is it genetic?
The cause and inheritance of Pai syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Pai syndrome can explain what it means for you and your family.
I was just diagnosed with Pai syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Pai syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Pai syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Pai syndrome, filtered to your area.
Are there clinical trials for Pai syndrome?
Tomeko shows live, recruiting studies for Pai syndrome from ClinicalTrials.gov on the hub.
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