Hammerstein W, Meiers H G, Haensch R
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1975 Jun 6;195(3):161-73. doi: 10.1007/BF00410468.
The authors report about observations they made in two sisters. One sister showed a fibroid degeneration of the cornea, the other a band-shaped keratopathy respectively, together with an ichthyosis and an alopecia as a result of capillary fractures due to pili torti. An autosomal recessive hereditary transmission could be determined. The cutaneous lesion is either an ichthyosis vulgaris, the hereditary transmission of which could not yet be confirmed, or it is a transition form of ichthyosis vulgaris and congenita.
作者报告了他们在两姐妹身上所做的观察。一个姐妹表现为角膜纤维瘤变性,另一个表现为带状角膜病变,同时伴有寻常型鱼鳞病和因扭曲毛发导致的毛细血管断裂引起的脱发。可以确定为常染色体隐性遗传。皮肤病变要么是寻常型鱼鳞病,其遗传方式尚未得到证实,要么是寻常型鱼鳞病和先天性鱼鳞病的过渡形式。