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Noonan syndrome with multiple lentigines

Just diagnosed with Noonan syndrome with multiple lentigines?

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

Open the full Noonan syndrome with multiple lentigines hub →

Overview

Noonan syndrome with multiple lentigines is a rare condition. Also known as Cardiomyopathic lentiginosis, Familial multiple lentigines syndrome, LEOPARD syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Noonan syndrome with multiple lentigines so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:500 · OMIM 151100, 611554, 613707 · ICD-10 Q87.1 · GARD 0001100

Find care for Noonan syndrome with multiple lentigines

Authoritative references for Noonan syndrome with multiple lentigines

Common questions

I was just diagnosed with Noonan syndrome with multiple lentigines — what should I do first?

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

Where can I find a specialist for Noonan syndrome with multiple lentigines?

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

Are there clinical trials for Noonan syndrome with multiple lentigines?

Tomeko shows live, recruiting studies for Noonan syndrome with multiple lentigines 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