Hamm H, Happle R
Am J Med Genet. 1986 Aug;24(4):685-90. doi: 10.1002/ajmg.1320240413.
Inflammatory linear verrucous epidermal nevus (ILVEN) is a rare skin disease with characteristic clinical and histological changes. The approximately 100 cases so far reported include only one familial occurrence involving a woman and her nephew. We report the occurrence of typical ILVEN in a 47-year-old mother and her 17-year-old daughter. So far, no clear-cut genetic interpretation of this observation can be given. Apart from coincidence, various genetic explanations are considered, including X-linked inheritance with extreme lyonization.
炎症性线状疣状表皮痣(ILVEN)是一种具有特征性临床和组织学改变的罕见皮肤病。迄今为止报道的约100例病例中,仅有1例为家族性发病,涉及一名女性及其侄子。我们报告了一名47岁母亲和她17岁女儿患典型ILVEN的病例。到目前为止,对于这一观察结果尚无明确的遗传学解释。除了巧合之外,还考虑了各种遗传学解释,包括伴有极端莱昂化的X连锁遗传。