Just diagnosed with Renpenning syndrome?
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 interactive Renpenning syndrome hub →Overview
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
Find care for Renpenning syndrome
Authoritative references for Renpenning syndrome
Research & market landscape for Renpenning syndrome
Following Renpenning syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Renpenning syndrome — the real-world landscape behind the condition, in one place.
- Latest Renpenning syndrome research on PubMed ↗
- Recruiting Renpenning syndrome trials on ClinicalTrials.gov ↗
- Explore the Renpenning 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 Renpenning syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Renpenning syndrome?
Renpenning syndrome is a rare condition. Also known as X-linked intellectual disability due to PQBP1 mutations, X-linked intellectual disability, Renpenning type. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Renpenning syndrome together in one place.
What are the symptoms of Renpenning syndrome?
Symptoms of Renpenning 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 Renpenning syndrome.
How is Renpenning syndrome treated?
Treatment for Renpenning syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Renpenning syndrome, and review current options with them.
What causes Renpenning syndrome — is it genetic?
The cause and inheritance of Renpenning syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Renpenning syndrome can explain what it means for you and your family.
I was just diagnosed with Renpenning syndrome — what should I do first?
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.
Where can I find a specialist for Renpenning syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Renpenning syndrome, filtered to your area.
Are there clinical trials for Renpenning syndrome?
Tomeko shows live, recruiting studies for Renpenning syndrome from ClinicalTrials.gov on the hub.
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