易被误诊为肝炎的遗传代谢性肝病  

Genetic metabolic liver disease easily misdiagnosed as hepatitis

作　　者：朱世殊 董漪 ZHU Shi-shu;DONG Yi(Adolescent Liver Disease Center,5th Medical Center,PLA General Hospital,Beijing100039,China)

机构地区：[1]解放军总医院第五医学中心青少年肝病诊疗与研究中心,北京100039

出　　处：《中国实用儿科杂志》2020年第7期528-531,共4页Chinese Journal of Practical Pediatrics

摘　　要：遗传代谢性肝病为罕见病,种类多,总体患病人群并不少。早期临床表现与肝炎相似无特异性,常规检查难以确诊,易导致误诊。因此,临床上应从不明原因的肝病中早期识别这类疾病,及早行特殊检查,早诊断、早治疗,避免肝病进展。Genetic metabolic liver disease is a rare disease with many types and common populations.Early clinical manifestations are similar to those of hepatitis and are without specificity.Routine examination can hardly provide a confirmed diagnosis and is likely to lead to misdiagnosis.Therefore,in clinical practice,liver diseases of unknown causes should be identified early,special examination should be conducted as early as possible,and early diagnosis and early treatment should be made to avoid the progression of liver diseases.

关 键 词：遗传代谢性肝病 基因 肝炎 误诊 

分 类 号：R72[医药卫生—儿科]