DefinitionThis section has been translated automatically.
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.
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.
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Incoming links (5)
Bazex-dupré-reilhac syndrome; Comel-netherton syndrome; Erythème desquamative en plaque congénital et familial; Erythrodermia papillaris et reticularis; Erythrokeratodermia papillaris et reticularis;Outgoing links (8)
ELOVL4 gene; Erythème desquamative en plaque congénital et familial; Erythrokeratodermia figurata variabilis; Erythrokeratodermia papillaris et reticularis; Erythrokeratodermia progressive symmetrica; GJB3 Gene; GJB4 Gene; Loricrin gene ;Disclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
Prof. Dr. med. Peter Altmeyer