tomeko

17p11.2 microduplication syndrome

Just diagnosed with 17p11.2 microduplication syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 17p11.2 microduplication syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full 17p11.2 microduplication syndrome hub →

Overview

17p11.2 microduplication syndrome is a rare condition. Also known as Potocki-Lupski syndrome, Trisomy 17p11.2. Tomeko brings together the specialists, research, clinical trials, treatments and community for 17p11.2 microduplication syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:1713 · OMIM 610883 · ICD-10 Q92.3 · GARD 0010145

Find care for 17p11.2 microduplication syndrome

Authoritative references for 17p11.2 microduplication syndrome

Common questions

I was just diagnosed with 17p11.2 microduplication syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 17p11.2 microduplication syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 17p11.2 microduplication syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 17p11.2 microduplication syndrome, filtered to your area.

Are there clinical trials for 17p11.2 microduplication syndrome?

Tomeko shows live, recruiting studies for 17p11.2 microduplication 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