Tuberous sclerosis complex associated with dyschromatosis Tuberous sclerosis complex associated with dyschromatosis Tuberous sclerosis complex associated with dyschromatosis Tuberous sclerosis complex associated with dyschromatosis Tuberous sclerosis complex associated with dyschromatosis

Tuberous sclerosis is an autosomal dominant disease due to mutations in two genetic loci, characterized by hamartoma formation in the skin, nervous system, heart, kidney, and other organs. Dyschromatosis universalis hereditaria is an autosomal dominant genodermatosis, characterized by small hyperpigmented and hypopigmented macules, uniformly distributed over the entire body. The face is rarely involved, and the palms, soles, and mucous membranes...