Just diagnosed with Mesomelia-synostoses syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Mesomelia-synostoses syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Mesomelia-synostoses syndrome hub →Overview
Mesomelia-synostoses syndrome is a rare condition. Also known as 8q13 microdeletion syndrome, Del(8)q(13), Mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type, Mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type, Monosomy 8q13, Verloes-David syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Mesomelia-synostoses syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2496 · OMIM 600383 · ICD-10 Q78.8 · GARD 0004302
Find care for Mesomelia-synostoses syndrome
Authoritative references for Mesomelia-synostoses syndrome
Research & market landscape for Mesomelia-synostoses syndrome
Following Mesomelia-synostoses syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Mesomelia-synostoses syndrome — the real-world landscape behind the condition, in one place.
- Latest Mesomelia-synostoses syndrome research on PubMed ↗
- Recruiting Mesomelia-synostoses syndrome trials on ClinicalTrials.gov ↗
- Explore the Mesomelia-synostoses 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 Mesomelia-synostoses syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Mesomelia-synostoses syndrome?
Mesomelia-synostoses syndrome is a rare condition. Also known as 8q13 microdeletion syndrome, Del(8)q(13), Mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type, Mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type, Monosomy 8q13, Verloes-David syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Mesomelia-synostoses syndrome together in one place.
What are the symptoms of Mesomelia-synostoses syndrome?
Symptoms of Mesomelia-synostoses 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 Mesomelia-synostoses syndrome.
How is Mesomelia-synostoses syndrome treated?
Treatment for Mesomelia-synostoses syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Mesomelia-synostoses syndrome, and review current options with them.
What causes Mesomelia-synostoses syndrome — is it genetic?
The cause and inheritance of Mesomelia-synostoses syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Mesomelia-synostoses syndrome can explain what it means for you and your family.
I was just diagnosed with Mesomelia-synostoses syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Mesomelia-synostoses syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Mesomelia-synostoses syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Mesomelia-synostoses syndrome, filtered to your area.
Are there clinical trials for Mesomelia-synostoses syndrome?
Tomeko shows live, recruiting studies for Mesomelia-synostoses syndrome from ClinicalTrials.gov on the hub.
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