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4p16.3 microduplication syndrome

Just diagnosed with 4p16.3 microduplication syndrome?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 4p16.3 microduplication syndrome, look for clinical trials, and connect with others living with it — all in one place.

Open the full 4p16.3 microduplication syndrome hub →

Overview

4p16.3 microduplication syndrome is a rare condition. Also known as Distal duplication 4p, Distal trisomy 4p, Telomeric duplication 4p, Trisomy 4pter. Tomeko brings together the specialists, research, clinical trials, treatments and community for 4p16.3 microduplication syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:96072 · ICD-10 Q92.3 · GARD 0019306

Find care for 4p16.3 microduplication syndrome

Authoritative references for 4p16.3 microduplication syndrome

Common questions

I was just diagnosed with 4p16.3 microduplication syndrome — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 4p16.3 microduplication syndrome, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 4p16.3 microduplication syndrome?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 4p16.3 microduplication syndrome, filtered to your area.

Are there clinical trials for 4p16.3 microduplication syndrome?

Tomeko shows live, recruiting studies for 4p16.3 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