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KBG syndrome

Just diagnosed with KBG syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees KBG syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full KBG syndrome hub →

Overview

KBG syndrome is a rare condition. Also known as ANKRD11-related disorder, Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for KBG syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:2332 · OMIM 148050 · ICD-10 Q87.8 · GARD 0000082

Find care for KBG syndrome

Authoritative references for KBG syndrome

Common questions

I was just diagnosed with KBG syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees KBG syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for KBG syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat KBG syndrome, filtered to your area.

Are there clinical trials for KBG syndrome?

Tomeko shows live, recruiting studies for KBG 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