11.1黄疸(英文课件)课件.pptVIP

1.Gilber syndrome:hepatocyte uptaking UCB abnormal, deficiency of glucuronyl transferase, →UCB↑ →jaundice (no symptom,liver function normal). 2.Dubin-Johnson’s syndrome:abnormal of Hepatocyte excreting CB and some anion to bile capillary →CB↑ →jaundice. 3.Crigler-Najjar’s syndrome:absence of glucuronyl transferase in hepatocyte, UCB can’t be transfered to CB，serum UCB↑→jaundice,UCB↑↑↑→nuclear jaundic, newborn,poor prediction. 4.Rotor’s syndrome:deficiency of Hepatocyte uptaking UCB and excreting CB,→bilirubin↑→jaundice. * Accessory Examination 1.Ultrosound 2.X ray 3.ERCP(Endoscopic retrograd