Erythrokeratodermia Variabilis
An autosomal dominant skin disease characterized by transient and variable noninflammatory ERYTHEMA and hyperkeratosis. It has been associated with mutations in the genes that code for CONNEXINS. Erythrokeratodermia variabilis inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA.
Year introduced: 2010
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Subheadings:
Tree Number(s): C16.320.850.337, C17.800.229.606, C17.800.428.304, C17.800.827.337
MeSH Unique ID: D056266
Entry Terms:
- Mendes De Costa Syndrome
- Erythrokeratodermia Variabilis with Erythema Gyratum Repens
- Erythro et Keratodermia Variabilis
- Erythrokeratodermia, Progressive Symmetric
- Progressive Symmetric Erythrokeratodermia
- Erythrokeratodermia Figurata, Congenital Familial, in Plaques
- Erythrokeratodermia Figurata Variabilis
- Greither Disease
- Transgrediens et Progrediens Palmoplantar Keratoderma
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