Verbov J
Br J Dermatol. 1975 Apr;92(4):469-74. doi: 10.1111/j.1365-2133.1975.tb03110.x.
A nulliparous female aged 26 years, who presented with long-standing sore and cracked soles, showed congenital anonychia, long-standing hyper-and-hypo-pigmentation in axillae and groins, dry palmar and plantar skin as well as other skin and hair abnormalities. She gave a family history of nail, hair and pigmentary abnormalities and examination of living affected relatives confirmed this. This appears to be a hitherto undescribed autosomal dominant syndrome.
一名26岁的未育女性,因长期足底疼痛和皲裂前来就诊,检查发现其患有先天性无甲症,腋窝和腹股沟存在长期的色素沉着过度和色素沉着不足,手掌和足底皮肤干燥,以及其他皮肤和毛发异常。她有指甲、毛发和色素异常的家族史,对在世的患病亲属进行检查证实了这一点。这似乎是一种迄今未被描述的常染色体显性综合征。