1Ichikawa T, Hiraga Y. A previously undescrided anomaly of pigmentation dyschromatosis universalis hereditaria [J]. Jpn J Dermatol, 1933, 34:360-364.
2Yang JH, Wong CK. Dyschromatosis universalis with X-linked ocular albinism [J]. Clin Exp Dermatol, 1991, 16(6): 436-440.
3Shono S, Toda K. Universal dyschromatosis associated with photosensitivity and neurosensory hearing defect [J]. Arch Der matol, 1990, 126(12):1659-1660.
4Pavithran K. Dyschromatosis universalis hereditaria with epilepsy[J]. Indian J Dermatol Venereol Leprol, 1991, 57(2):102-103.
5Nordlund JJ,Howanitz N, Hearing V, et al. The PigmentarySystem: Physiology and Pathology[M]. New York: Oxford Uni versity Press, 1998. 724-726.
6Yamada T, Shinojima H. Case Presentation XVI International Congress of Dermatology [M]. Tokyo: University of Tokyo Press, 1982. 141.
7Oyama M, Shimizu H, Ohata Y, et al. Dyschromatosis symmet rica hereditaria(reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases [J]. Br J Dernatol, 1999, 140(3): 491-496.
8Urabe K, Hori Y. Dyschromatosis [J]. Semin Cutan Med Surg, 1997, 16(1):81-85.
