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.

Also Known As:

Erythro et Keratodermia Variabilis; Erythrokeratodermia Figurata, Congenital Familial, in Plaques; Erythrokeratodermia Variabilis with Erythema Gyratum Repens; Erythrokeratodermia, Progressive Symmetric; Transgrediens et Progrediens Palmoplantar Keratoderma; Progressive Symmetric Erythrokeratodermia; Erythrokeratodermia Figurata Variabilis; Greither Disease; Mendes De Costa Syndrome

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Erythrokeratodermia Variabilis: 57
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Erythema: 8083
    - Erythrokeratodermia Variabilis: 57
  - Keratosis: 706
    - Erythrokeratodermia Variabilis: 57
  - Genetic Skin Diseases: 47
    - Erythrokeratodermia Variabilis: 57

Fai Yan Fang Selected Research

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Disease

Drug/Important Bio-Agent (IBA)