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Grubben-de Cock-Borghgraef syndrome

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.

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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

Common questions

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.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com