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Fuhrmann syndrome

Just diagnosed with Fuhrmann syndrome?

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

Open the full Fuhrmann syndrome hub →

Overview

Fuhrmann syndrome is a rare condition. Also known as Fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome, Fuhrmann-Rieger-de Sousa syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Fuhrmann syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:2854 · OMIM 228930 · ICD-10 Q74.8 · GARD 0002410

Find care for Fuhrmann syndrome

Authoritative references for Fuhrmann syndrome

Common questions

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

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

Where can I find a specialist for Fuhrmann syndrome?

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

Are there clinical trials for Fuhrmann syndrome?

Tomeko shows live, recruiting studies for Fuhrmann 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