Yañez S, Velasco J A, González M P
Department of Dermatology, Clinical Hospital, University of Salamanca, Spain.
Clin Exp Dermatol. 1993 May;18(3):283-5. doi: 10.1111/j.1365-2230.1993.tb02190.x.
Two cases of erythromelanosis follicularis faciei et colli in one family, affecting a brother and sister are described. In these cases erythromelanosis follicularis faciei et colli, a process of unknown aetiology, seems to have a clear hereditary component--autosomal recessive mode of inheritance--a feature which, as far as we know, has not been reported in the literature.
本文描述了一个家族中两例面部和颈部毛囊性红斑黑变病的病例，患者为一名兄弟和一名姐妹。在这些病例中，病因不明的毛囊性红斑黑变病似乎有明显的遗传因素——常染色体隐性遗传模式——就我们所知，这一特征在文献中尚未有报道。
