You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant epidermolytic ichthyosis, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant epidermolytic ichthyosis hub →Autosomal dominant epidermolytic ichthyosis is a rare condition. Also known as BCIE, Bullous congenital ichthyosiform erythroderma, Bullous congenital ichthyosiform erythroderma of Brock, Bullous ichthyosis, EHK, EI, Epidermolytic hyperkeratosis, Ichthyosis hystrix Brocq type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant epidermolytic ichthyosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:312 · OMIM 113800, 620150 · ICD-10 Q80.3 · GARD 0001039
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant epidermolytic ichthyosis, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Autosomal dominant epidermolytic ichthyosis, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant epidermolytic ichthyosis from ClinicalTrials.gov on the hub.