Just diagnosed with Grubben-de Cock-Borghgraef syndrome?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Grubben-de Cock-Borghgraef syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Grubben-de Cock-Borghgraef syndrome hub →Overview
Grubben-de Cock-Borghgraef syndrome is a rare condition. Also known as Developmental delay-hypotonia-extremities hypertrophy syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Grubben-de Cock-Borghgraef syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2101 · OMIM 233810 · ICD-10 Q87.8 · GARD 0002576
Find care for Grubben-de Cock-Borghgraef syndrome
Authoritative references for Grubben-de Cock-Borghgraef syndrome
Research & market landscape for Grubben-de Cock-Borghgraef syndrome
Following Grubben-de Cock-Borghgraef syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Grubben-de Cock-Borghgraef syndrome — the real-world landscape behind the condition, in one place.
- Latest Grubben-de Cock-Borghgraef syndrome research on PubMed ↗
- Recruiting Grubben-de Cock-Borghgraef syndrome trials on ClinicalTrials.gov ↗
- Explore the Grubben-de Cock-Borghgraef syndrome research & specialist footprint on Tomeko
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Common questions
What is Grubben-de Cock-Borghgraef syndrome?
Grubben-de Cock-Borghgraef syndrome is a rare condition. Also known as Developmental delay-hypotonia-extremities hypertrophy syndrome. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Grubben-de Cock-Borghgraef syndrome together in one place.
What are the symptoms of Grubben-de Cock-Borghgraef syndrome?
Symptoms of Grubben-de Cock-Borghgraef 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 Grubben-de Cock-Borghgraef syndrome.
How is Grubben-de Cock-Borghgraef syndrome treated?
Treatment for Grubben-de Cock-Borghgraef syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Grubben-de Cock-Borghgraef syndrome, and review current options with them.
What causes Grubben-de Cock-Borghgraef syndrome — is it genetic?
The cause and inheritance of Grubben-de Cock-Borghgraef syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Grubben-de Cock-Borghgraef syndrome can explain what it means for you and your family.
I was just diagnosed with Grubben-de Cock-Borghgraef syndrome — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Grubben-de Cock-Borghgraef syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Grubben-de Cock-Borghgraef syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Grubben-de Cock-Borghgraef syndrome, filtered to your area.
Are there clinical trials for Grubben-de Cock-Borghgraef syndrome?
Tomeko shows live, recruiting studies for Grubben-de Cock-Borghgraef syndrome from ClinicalTrials.gov on the hub.
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