#erythrokeratodermia_variabilis
Erythrokeratodermia variabilis
Medical condition
Erythrokeratodermia variabilis is a rare autosomal dominant disorder that usually presents at birth or during the first year of life. To date, it is thought to be caused by mutations in genes encoding for connexin channels proteins in the epidermis, leading to the misregulation of homeostasis in keratinocytes.
Wed 25th
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