Erythrokeratoderma (overview)

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.10.2020

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Group of rare, autosomal dominant, inherited inflammatory ichthyoses clinically characterized by mostly variable erythema and sharply limited hyperkeratoses, as well as mutations of the transmembrane protein connexin 30.3 or 31.


Please ask your physician for a reliable diagnosis. This website is only meant as a reference.


Last updated on: 29.10.2020