You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Focal facial dermal dysplasia type I, look for clinical trials, and connect with others living with it — all in one place.
Open the full Focal facial dermal dysplasia type I hub →Focal facial dermal dysplasia type I is a rare condition. Also known as Bitemporal aplasia cutis congenita, Brauer syndrome, FFDD type I, FFDD1, Focal facial dermal dysplasia 1, Brauer type, Focal facial dermal dysplasia type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Focal facial dermal dysplasia type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79133 · OMIM 136500 · ICD-10 Q82.8 · GARD 0016524
Start by learning the basics from an authoritative source, find a specialist or center that sees Focal facial dermal dysplasia type I, 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 Focal facial dermal dysplasia type I, filtered to your area.
Tomeko shows live, recruiting studies for Focal facial dermal dysplasia type I from ClinicalTrials.gov on the hub.