neonatal hepatitis syndrome

Alteration of plasma α _1-antichymotrypsin in neonatal hepatitis syndrome and its clinical significance

35例新生儿肝炎综合征血浆α1-ACT变化及其临床意义初探

Some gene mutations may increase the TTV pathogen , and result in neonatal hepatitis syndrome or hyperbilirubinemia .

结论TTV中国株与日本株具有同源性，某些TTV基因突变可增强其致病性，可导致新生儿肝功能损害和结合胆红素升高。

Among them 21 patients were changed to neonatal hepatitis syndrome . DETECTION OF CYTOMEGALOVIRUS IN NEONATAL HEPATITIS SYNDROME BY POLYMERASE CHAIN REACTION

21例转为新生儿肝炎综合征。PCR检测婴儿肝炎综合征中巨细胞病毒感染

We use the technique of PCR and ECL to detect urine HCMV-DNA of neonatal hepatitis syndrome . The positive rates are 66 . 7 % and 53 . 3 % respectively , positive rate of control group is 14 . 3 % .

本文应用PCR及ECL技术检测新生儿肝炎综合征患儿尿液中的HCMV－DNA，阳性率分别为66.7%及53.3%，对照组为14.3%。

Diagnosis and treatment of neonatal and infantile hepatitis syndrome

新生儿和婴儿肝炎综合征的诊断与处理

Relationship between TORCH Infection and Neonatal and Infantile Hepatitis Syndrome

TORCH感染与新生儿及婴儿肝炎综合征的关系

Objective To study the attack of TORCH infections in neonatal and infantile hepatitis syndrome .

目的探讨TORCH感染在新生儿、婴儿肝炎综合征发病中的作用。