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Meacham syndrome

Just diagnosed with Meacham syndrome?

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

Open the full Meacham syndrome hub →

Overview

Meacham syndrome is a rare condition. Also known as Meacham-Winn-Culler syndrome, Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Meacham syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:3097 · OMIM 608978 · ICD-10 Q87.8 · GARD 0003432

Find care for Meacham syndrome

Authoritative references for Meacham syndrome

Common questions

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

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

Where can I find a specialist for Meacham syndrome?

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

Are there clinical trials for Meacham syndrome?

Tomeko shows live, recruiting studies for Meacham 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