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鱼鳞病中的血清类固醇硫酸盐。

Serum steroid sulphates in ichthyosis.

作者信息

Ruokonen A, Oikarinen A, Palatsi R, Huhtaniemi I

出版信息

Br J Dermatol. 1980 Sep;103(3):245-8. doi: 10.1111/j.1365-2133.1980.tb07240.x.

Abstract

Serum concentrations of pregnenolone sulphate, dehydroepiandrosterone sulphate and 5-androstene-3 beta,17 beta-diol sulphate were measured by radioimmunoassays in twelve patients with various types of ichthyosis. In X-linked ichthyosis (n = 5), ichthyosis vulgaris (n = 5) and lamellar ichthyosis (n = 1), steroid sulphates were not significantly higher than in the control subjects. In one baby with ichthyosiform erythroderma and associated deafness serum 5 -androstene-3 beta,17 beta-diol sulphate concentration was about 60 fold higher (31 microgram/ml) than the mean of the control children. The other steroid sulphate levels were normal in this baby. These results indicate that it is not possible to demonstrate the steroid sulphatase deficiency in X-linked ichthyosis by determining blood steroid sulphates. The cause of the high 5-androstene-3 beta,17 beta-diol sulphate concentration in the baby with ichthyosiform erythroderma needs further evaluation.

摘要

通过放射免疫分析法测定了12例不同类型鱼鳞病患者血清中硫酸孕烯醇酮、硫酸脱氢表雄酮和硫酸5-雄烯-3β,17β-二醇的浓度。在X连锁鱼鳞病(n = 5)、寻常型鱼鳞病(n = 5)和板层状鱼鳞病(n = 1)患者中,类固醇硫酸盐水平并不显著高于对照组。在1例患有鱼鳞病样红皮病并伴有耳聋的婴儿中,血清硫酸5-雄烯-3β,17β-二醇浓度比对照儿童的平均值高约60倍(31微克/毫升)。该婴儿的其他类固醇硫酸盐水平正常。这些结果表明,通过测定血液中的类固醇硫酸盐无法证实X连锁鱼鳞病中类固醇硫酸酯酶缺乏。患有鱼鳞病样红皮病的婴儿中硫酸5-雄烯-3β,17β-二醇浓度升高的原因需要进一步评估。

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