Just diagnosed with Familial keratoacanthoma?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial keratoacanthoma, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Familial keratoacanthoma hub →Overview
Familial keratoacanthoma is a rare condition. Also known as Hereditary keratoacanthoma, Multiple keratoacanthoma. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial keratoacanthoma so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:493 · ICD-10 L85.8 · GARD 0018693
Find care for Familial keratoacanthoma
Authoritative references for Familial keratoacanthoma
Research & market landscape for Familial keratoacanthoma
Following Familial keratoacanthoma for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Familial keratoacanthoma — the real-world landscape behind the condition, in one place.
- Latest Familial keratoacanthoma research on PubMed ↗
- Recruiting Familial keratoacanthoma trials on ClinicalTrials.gov ↗
- Explore the Familial keratoacanthoma 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 Familial keratoacanthoma and every rare condition. See how Tomeko works with industry →
Common questions
What is Familial keratoacanthoma?
Familial keratoacanthoma is a rare condition. Also known as Hereditary keratoacanthoma, Multiple keratoacanthoma. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Familial keratoacanthoma together in one place.
What are the symptoms of Familial keratoacanthoma?
Symptoms of Familial keratoacanthoma 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 Familial keratoacanthoma.
How is Familial keratoacanthoma treated?
Treatment for Familial keratoacanthoma depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Familial keratoacanthoma, and review current options with them.
What causes Familial keratoacanthoma — is it genetic?
The cause and inheritance of Familial keratoacanthoma are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Familial keratoacanthoma can explain what it means for you and your family.
I was just diagnosed with Familial keratoacanthoma — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial keratoacanthoma, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Familial keratoacanthoma?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Familial keratoacanthoma, filtered to your area.
Are there clinical trials for Familial keratoacanthoma?
Tomeko shows live, recruiting studies for Familial keratoacanthoma from ClinicalTrials.gov on the hub.
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