Suppr超能文献

Distribution of serum amylase isoenzymes in cystic fibrosis homozygotes and heterozygotes.

作者信息

Takács O, Sohár I, László A, Pénzes P, Gyurkovits K

出版信息

Acta Paediatr Acad Sci Hung. 1977;18(1):21-6.

PMID:602748
Abstract

A simple method has been elaborated for the routine separation and quantitative determination of amylase isoenzymes. The ratio P/S, the quotient of the activity values obtained by densitometric evaluation of the pancreatic and salivary isoenzymes, is used to characterize their distribution. In healthy adults and children the value for P/S is above 1 in 80% of the cases, with a mean of 1.87 +/- 0.23. In 90% of heterozygote CF gene-carriers, the P/S is below 1 with a mean of 0.68 +/- 0.13. In addition to the higher total amylase activity, in MV homozygote patients P/S is less than 0.1, and even 0.001. The phenomenon is explained by a compensatory enhancement of salivary activity. The method is a suitable diagnostic test of the exocrine function of the pancreas and for evaluation of the serum amylase isoenzymes. The P/S value allows to differentiate heterozygote CF gene-carriers from homozygotes and healthy individuals.

摘要

相似文献

6
Cystic fibrosis: a HLA associated hereditary disease?
Acta Paediatr Acad Sci Hung. 1977;18(1):27-9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验