Just diagnosed with Scleromyxedema?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Scleromyxedema, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Scleromyxedema hub →Overview
Scleromyxedema is a rare condition. Also known as Arndt-Gottron disease, Generalized lichenoid papular eruption, Generalized papular and sclerodermoid lichen myxedematosus. Tomeko brings together the specialists, research, clinical trials, treatments and community for Scleromyxedema so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:167635 · ICD-10 L98.5 · GARD 0007615
Find care for Scleromyxedema
Authoritative references for Scleromyxedema
Research & market landscape for Scleromyxedema
Following Scleromyxedema for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Scleromyxedema — the real-world landscape behind the condition, in one place.
- Latest Scleromyxedema research on PubMed ↗
- Recruiting Scleromyxedema trials on ClinicalTrials.gov ↗
- Explore the Scleromyxedema research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Scleromyxedema and every rare condition. See how Tomeko works with industry →
Common questions
What is Scleromyxedema?
Scleromyxedema is a rare condition. Also known as Arndt-Gottron disease, Generalized lichenoid papular eruption, Generalized papular and sclerodermoid lichen myxedematosus. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Scleromyxedema together in one place.
What are the symptoms of Scleromyxedema?
Symptoms of Scleromyxedema vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Scleromyxedema.
How is Scleromyxedema treated?
Treatment for Scleromyxedema depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Scleromyxedema, and review current options with them.
What causes Scleromyxedema — is it genetic?
The cause and inheritance of Scleromyxedema are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Scleromyxedema can explain what it means for you and your family.
I was just diagnosed with Scleromyxedema — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Scleromyxedema, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Scleromyxedema?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Scleromyxedema, filtered to your area.
Are there clinical trials for Scleromyxedema?
Tomeko shows live, recruiting studies for Scleromyxedema from ClinicalTrials.gov on the hub.
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