Erythrokeratoderma

Erythroketoderma is a rare hereditary skin disease caused by mutations in the KMT-3 gene, which is characterized by multiple hyperpigmented acral lesions of keratoconidia and skin atrophy with sensitive areas. Erythrokeratosis of the scalp and palms

Erythrokeratosis is a group of hereditary skin diseases characterized by thickening of the stratum corneum, changes in its color and the formation of raised elements. In recent years, the diagnosis of erythrokeratosis has begun to be clarified, and clear diagnostic criteria have been developed. Treatment of erythrodysemiform dermatitis