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This case report describes a 5-year-old boy with extensive epidermal nevus who experienced marked improvement using a topical calcipotriol/betamethasone dipropionate combination ointment.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

This letter to the editor discusses the natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family but does not present new clinical results.