Just diagnosed with Patterson-Stevenson-Fontaine syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Patterson-Stevenson-Fontaine syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Patterson-Stevenson-Fontaine syndrome hub →Overview
Patterson-Stevenson-Fontaine syndrome is a rare condition. Also known as Patterson-Stevenson syndrome, Split foot deformity-mandibulofacial dysostosis syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Patterson-Stevenson-Fontaine syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2439 · OMIM 183700 · ICD-10 Q87.0 · GARD 0004260
Find care for Patterson-Stevenson-Fontaine syndrome
Authoritative references for Patterson-Stevenson-Fontaine syndrome
Research & market landscape for Patterson-Stevenson-Fontaine syndrome
Following Patterson-Stevenson-Fontaine syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Patterson-Stevenson-Fontaine syndrome — the real-world landscape behind the condition, in one place.
- Latest Patterson-Stevenson-Fontaine syndrome research on PubMed ↗
- Recruiting Patterson-Stevenson-Fontaine syndrome trials on ClinicalTrials.gov ↗
- Explore the Patterson-Stevenson-Fontaine 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 Patterson-Stevenson-Fontaine syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Patterson-Stevenson-Fontaine syndrome?
Patterson-Stevenson-Fontaine syndrome is a rare condition. Also known as Patterson-Stevenson syndrome, Split foot deformity-mandibulofacial dysostosis syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Patterson-Stevenson-Fontaine syndrome together in one place.
What are the symptoms of Patterson-Stevenson-Fontaine syndrome?
Symptoms of Patterson-Stevenson-Fontaine 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 Patterson-Stevenson-Fontaine syndrome.
How is Patterson-Stevenson-Fontaine syndrome treated?
Treatment for Patterson-Stevenson-Fontaine syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Patterson-Stevenson-Fontaine syndrome, and review current options with them.
What causes Patterson-Stevenson-Fontaine syndrome — is it genetic?
The cause and inheritance of Patterson-Stevenson-Fontaine syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Patterson-Stevenson-Fontaine syndrome can explain what it means for you and your family.
I was just diagnosed with Patterson-Stevenson-Fontaine syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Patterson-Stevenson-Fontaine syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Patterson-Stevenson-Fontaine syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Patterson-Stevenson-Fontaine syndrome, filtered to your area.
Are there clinical trials for Patterson-Stevenson-Fontaine syndrome?
Tomeko shows live, recruiting studies for Patterson-Stevenson-Fontaine syndrome from ClinicalTrials.gov on the hub.
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