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 Mesomelia-synostoses syndrome hub →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
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.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Mesomelia-synostoses syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Mesomelia-synostoses syndrome from ClinicalTrials.gov on the hub.