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Multiple synostosis syndrome

Just diagnosed with Multiple synostosis syndrome?

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

Open the full Multiple synostosis syndrome hub →

Overview

Multiple synostosis syndrome is a rare condition. Also known as Deafness-Hermann type symphalangism syndrome, Facio-audio-symphalangism, Hearing loss-Hermann type symphalangism syndrome, Symphalangism-brachydactyly syndrome, WL syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Multiple synostosis syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:3237 · OMIM 186500, 610017, 612961 · ICD-10 Q78.8 · GARD 0003836

Find care for Multiple synostosis syndrome

Authoritative references for Multiple synostosis syndrome

Common questions

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

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

Where can I find a specialist for Multiple synostosis syndrome?

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

Are there clinical trials for Multiple synostosis syndrome?

Tomeko shows live, recruiting studies for Multiple synostosis 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