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.
Erythrokeratoderma (overview)
DefinitionThis section has been translated automatically.
ClassificationThis section has been translated automatically.
These include:
- Erythrokeratodermia figurata variabilis (connexin genes GJB3 and GJB4)
- Erythrokeratodermia papillaris et reticularis
- Erythrokeratodermia progressiva symmetrica (mutations in the genes ELOVL4, loricrin and in various connexin genes)
- Erythème desquamative en plaque congénital et familial.