Gilbert综合征又名先天性非溶血性黄疸(间接胆红素增高型)。临床较少见,常易误诊为“肝炎”或“胆道疾患”。我院遇到2例,报道如下。1 病例例1:男,20岁。劳累后间发巩膜黄染2年余,休息数天后自消,无厌油、腹痛等。多次肝功能检查仅有黄疸指数增高,诊断为“瘀胆型肝炎”,护肝 Gilbert syndrome, also known as congenital non-hemolytic jaundice (indirect bilirubin increased type). Clinical less common, often misdiagnosed as “hepatitis” or “biliary disorders.” I met two cases in hospital, reported as follows. Case 1: Male, 20 years old. After exertion hair scleral yellow dye more than 2 years, a few days after the self-elimination, no greasy oil, abdominal pain and so on. Multiple liver function tests only jaundice index increased, diagnosed as “stasis gallbladder hepatitis”, liver protection