Ocaña Sierra J, Blesa G, Montero E
Ann Dermatol Syphiligr (Paris). 1975;102(1):41-5.
Four cases of keratoma hereditaria mutilans (Vohwinkel syndrome) are reported in two families, whereas clinic, metabolic, radiologic, histologic and cytogenetic aspects, the association with other processes, and therapeutic possibilities.
本文报道了两个家族中的4例遗传性残毁性角皮瘤（Vohwinkel综合征）病例，并探讨了其临床、代谢、放射学、组织学和细胞遗传学特征，与其他疾病的关联以及治疗方法。
