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Loricrin keratoderma

Just diagnosed with Loricrin keratoderma?

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

Open the full Loricrin keratoderma hub →

Overview

Loricrin keratoderma is a rare condition. Also known as Camisa disease, Keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome, Loricrin keratoderma, Vohwinkel syndrome with ichthyosis. Tomeko brings together the specialists, research, clinical trials, treatments and community for Loricrin keratoderma so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:79395 · OMIM 604117 · ICD-10 Q82.8 · GARD 0016719

Find care for Loricrin keratoderma

Authoritative references for Loricrin keratoderma

Common questions

I was just diagnosed with Loricrin keratoderma — what should I do first?

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

Where can I find a specialist for Loricrin keratoderma?

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

Are there clinical trials for Loricrin keratoderma?

Tomeko shows live, recruiting studies for Loricrin keratoderma 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