نتایج جستجو برای: recurrent cholestasis

تعداد نتایج: 134921  

Journal: :acta medica iranica 0
kavehmanesh z kosari f

this report presents an 11 year-old girl with benign recurrent cholestasis (bric) who developed episodes of severe jaundice and pruritus at the ages of 2.5 and 10 years. each episode lasted for 3-4 months. the peak level of serum bilirubin reached 33-37 mg/dl.liver function tests were all normal during the attack except for increased alkaline phosphatase and prolonged prothrombin time responsiv...

Journal: :middle east journal of digestive diseases 0
alireaz norouzi sadaf ghajarieh sepanlou samaneh tavassoli reza malekzadeh

0

Journal: :Gut 1978
G P van Berge-Henegouwen D R Ferguson A F Hofmann A G De Pagter

To determine whether a defect in uptake of organic anions is present in patients with benign recurrent cholestasis, the plasma disappearance of simultaneously injected indocyanine green and cholyglycine-1-14C was measured in eight patients with asymptomatic benign recurrent cholestasis, four with the familial type, as well as 22 healthy control subjects. Evans blue was also simultaneously injec...

2017
Su Jeong Lee Jung Eun Kim Byung-Ho Choe An Na Seo Han-Ik Bae Su-Kyeong Hwang

PURPOSE The goal of this study was the early diagnosis of ABCB11 spectrum liver disorders, especially those focused on benign recurrent intrahepatic cholestasis and progressive familial intrahepatic cholestasis. METHODS Fifty patients presenting neonatal cholestasis were evaluated to identify underlying etiologies. Genetic analysis was performed on patients suspected to have syndromic disease...

Journal: :Journal of the Royal Society of Medicine 1985

2017
Yi‐Ling Qiu Jing‐Yu Gong Jia‐Yan Feng Ren‐Xue Wang Jun Han Teng Liu Yi Lu Li‐Ting Li Mei‐Hong Zhang Jonathan A. Sheps Neng‐Li Wang Yan‐Yan Yan Jia‐Qi Li Lian Chen Christoph H. Borchers Bence Sipos A.S. Knisely Victor Ling Qing‐He Xing Jian‐She Wang

Hereditary cholestasis in childhood and infancy with normal serum gamma-glutamyltransferase (GGT) activity is linked to several genes. Many patients, however, remain genetically undiagnosed. Defects in myosin VB (MYO5B; encoded by MYO5B) cause microvillus inclusion disease (MVID; MIM251850) with recurrent watery diarrhea. Cholestasis, reported as an atypical presentation in MVID, has been consi...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2004
T Pérez Fernández P López Serrano E Tomás Ma L Gutiérrez J L Lledó G Cacho C Santander C M Fernández Rodríguez

When cholestatic liver disease is present, liver ultrasound should be performed to ascertain if cholestasis is extrahepatic or intrahepatic. If bile ducts appear dilated and the probability of interventional treatment is high, endoscopic retrograde cholagio-pancreatography (ERCP) or trans-hepatic cholangiography (THC) should be the next step. If the probability of interventional therapeutics is...

Journal: :Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 2003
Ziv Ben-Ari Orit Pappo Eytan Mor

Cholestasis is a common sequela of liver transplantation. Although the majority of cases remain subclinical, severe cholestasis may be associated with irreversible liver damage, requiring retransplantation. Therefore, it is essential that clinicians be able to identify and treat the syndromes associated with cholestasis. In this review, we consider causes of intrahepatic cholestasis. These may ...

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