探索线粒体病患儿毛发和皮肤的异常表现,以便与其它易混淆的疾病加以鉴别,达到早期诊断的目的。病人和方法　对巴黎某医院近10年经儿科和皮肤科医师仔细检查的140名10岁以内的线粒体病儿进行观察。所有患儿早期表现为不能解释的无关组织的复合症状。通过代谢筛查考虑到氧?.. To explore the abnormalities of hair and skin in children with mitochondrial diseases so as to distinguish them from other confusing diseases so as to achieve the purpose of early diagnosis. Patients and Methods A total of 140 children under the age of 10 with mitochondrial disease were examined at a hospital in Paris for nearly 10 years and were carefully examined by pediatric and dermatologists. Early manifestation of all children with unexplained complex symptoms of unrelated tissues. Consider oxygen through metabolic screening?