表皮松解性角化过度
角化过度
皮肤病科
角蛋白
乳头状瘤病
医学
角蛋白6A
角化不良
病理
痣
遗传性皮肤病
鱼鳞病
红皮病
生物
遗传学
癌症研究
基因
中间灯丝
黑色素瘤
细胞骨架
细胞
作者
Keiichi Uchiyama,Gen Nakanishi,Noriki Fujimoto,Mikiko Takikita,Toshihiro Tanaka
标识
DOI:10.1684/ejd.2013.2088
摘要
Epidermal nevus presents histologically with epidermal hyperplasia, hyperkeratosis, papillomatosis and, rarely, epidermolytic hyperkeratosis or granular degeneration. Mutations of keratin 1 and keratin 10 genes have been reported in epidermolytic ichthyosis [1], (previously called bullous congenital ichthyosiform erythroderma) [2], which shows epidermolytic hyperkeratosis. Genetic mosaicism has been reported in epidermal nevus with epidermolytic hyperkeratosis [3], where mutations of keratin 1 or [...]
科研通智能强力驱动
Strongly Powered by AbleSci AI