Koppe G, Marinković-Ilsen A, Rijken Y, De Groot W P, Jöbsis A C
Arch Dis Child. 1978 Oct;53(10):803-6. doi: 10.1136/adc.53.10.803.
In 3 pregnant women oestrogen excretion in the urine was very low. The pregnancies were otherwise uncomplicated and the 3 infants, boys, were normal at birth, but later developed ichthyosis of the X-linked inherited type. Histochemically, the placenta in each case showed deficiency in arylsulphatase-type C activity. In all three children the skin showed the same enzyme deficiency. In the skin of 9 other unrelated (adult) patients with proved X-linked inherited ichthyosis vulgaris, arylsulphatase C activity was deficient. Skin from 5 normal adults and 5 normal children showed arylsulphatase C activity to be present. It is concluded that a sulphatase deficiency is a factor in the causation of ichthyosis of the X-linked inherited type.
在3名孕妇中,尿中雌激素排泄量极低。这些妊娠在其他方面并无并发症,3名婴儿均为男孩,出生时正常,但后来患上了X连锁遗传型鱼鳞病。组织化学检查显示,每例病例中的胎盘均表现出芳基硫酸酯酶C型活性缺乏。在所有3名儿童中,皮肤也表现出相同的酶缺乏。在另外9名经证实患有X连锁遗传性寻常鱼鳞病的无关(成年)患者的皮肤中,芳基硫酸酯酶C活性也缺乏。5名正常成年人和5名正常儿童的皮肤显示存在芳基硫酸酯酶C活性。得出的结论是,硫酸酯酶缺乏是X连锁遗传型鱼鳞病病因中的一个因素。