Conclusion The inheritance mode of AAID is mitochondrial inheritance. Aminoglycoside antibiotic therapy should be avoided in those persons with a family history of AAID, especially their maternal relatives.
结论AAID属线粒体遗传,对具有AAID家族史的个体(尤其是母系亲属),应当避免使用氨基甙类抗生素。
The incidence of the 1555 A → G mutation in AAID and matrilineal non syndromic deafness pedigrees is fairly high.
1555A→G突变在西南地区AAID及非综合征性耳聋家系均有较高发生率。
Objective: The experiment was designed to research the relationship between mitochondrial DNA ( mtDNA) mutation and aminoglycoside antibiotic induced deafness ( AAID) and establish a gene diagnostic method.
目的:研究线粒体DNA突变与氨基糖甙类抗生素致聋(AAID)的关系,建立相应的基因诊断方法。
简答网 · 英语词汇
简答网 · 初中英语作文
简答网 · 双语娱乐资讯
简答网 · 高考英语
简答网 · 中考英语