粒线体疾病
疾病
医学
产前诊断
多学科方法
病理
怀孕
重症监护医学
生物信息学
线粒体DNA
生物
胎儿
遗传学
社会科学
基因
社会学
标识
DOI:10.1007/s10024-004-5051-4
摘要
The diagnosis of mitochondrial disease is challenging and requires a multidisciplinary approach for investigation. Despite the complexity, a specific diagnosis can be achieved in many cases. A specific diagnosis may provide prognostic information for the patient and the option of prenatal testing for the family in a subsequent pregnancy. the case reports in this section nicely illustrate several common pediatric clinical presentations of mitochondrial disease and a systematic approach to investigation.
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