You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Renpenning syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Renpenning syndrome hub →Renpenning syndrome is a rare condition. Also known as X-linked intellectual disability due to PQBP1 mutations, X-linked intellectual disability, Renpenning type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Renpenning syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:3242 · OMIM 309500 · ICD-10 Q87.5 · GARD 0009509
Start by learning the basics from an authoritative source, find a specialist or center that sees Renpenning 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 Renpenning syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Renpenning syndrome from ClinicalTrials.gov on the hub.