Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria

Dyschromatosis universalis hereditaria (DUH) is a very rare genodermatosis characterized by generalized hypopigmented and hyperpigmented macules of varying sizes and shapes occurring over almost all the body. It was first described in 1933 by Ichikawa and Higari. It is most commonly reported in Japan [ [1] Suenaga M. Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in five generations. Tohoku J Exp Med. 1952; 55:...