نتایج جستجو برای: recurrent cholestasis

تعداد نتایج: 134921  

Journal: :Frontiers in bioscience 2009
Emmanuel Gonzales Anne Davit-Spraul Christiane Baussan Catherine Buffet Michele Maurice Emmanuel Jacquemin

Class III multidrug resistance P-glycoproteins, mdr2 in mice and MDR3 in human, are canalicular phospholipid translocators involved in biliary phospholipid (phosphatidylcholine) excretion.The role of a MDR3 (ABCB4) gene defect in liver disease has been initially proven in a subtype of progressive familial intrahepatic cholestasis called PFIC3, a severe pediatric liver disease that may require l...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2003
Peter L Goering

A major function of the liver is the formation of bile and hepatobiliary excretion of endogenous substances and xenobiotics, such as chemicals, drugs, and their metabolites. Cholestasis is a general condition of multiple etiologies, hereditary and acquired, in which bile excretion from the liver is attenuated or blocked. In some forms of cholestasis, cholesterol metabolism is perturbed, resulti...

Journal: :The Yale Journal of Biology and Medicine 1967
Robert L. Scheig

JAUNDICE DURING PREGNANCY. By Urs Peter Haemmerli. New York, Springer-Verlag, Inc., 1967. 111 pp. $3.80, paperbound. Jaundice During Pregnancy is an excellent monograph which should be read by all internists, obstetricians, and pediatricians, and which should be available in all medical libraries for ready reference. The author concisely summarizes the known minor alterations of the liver and i...

2017
Ronghua Yu Yizhong Wang Yongmei Xiao Lili Mo Aishu Liu Dan Li Ting Ge Guangjun Yu Ting Zhang

Nutritional status of 380 hospitalised children aged from 1 month to 5 years with liver disease was evaluated in a single paediatric centre. The total prevalence of stunting (height-for-age Z (HAZ) < -2), underweight (weight-for-age Z (WAZ) < -2) and wasting (weight-for-height Z < -2) was 9·8, 9·0 and 7·9 %, respectively. The overall nutritional risk (-2 ≤ Z < -1) of stunting, underweight and w...

Journal: :Acta biochimica Polonica 2014
Aleksandra Lisowska Natalia Kobelska-Dubiel Irena Jankowska Joanna Pawłowska Jerzy Moczko Jarosław Walkowiak

BACKGROUND & AIMS To date, no studies concerning the presence of small intestinal bacterial overgrowth in patients with progressive familial intrahepatic cholestasis were published. Based upon characteristic of progressive familial intrahepatic cholestasis one can expect the coexistence of small intestinal bacterial overgrowth. The aim of the study was to assess the incidence of small intestina...

Journal: :Jornal de pediatria 2003
Marília D Bastos Themis R da Silveira

OBJECTIVE To verify blood levels of vitamin D in patients with chronic cholestasis, and relate them to nutritional status, length of time since the onset of cholestasis and use of vitamin supplement. METHODS Controlled cross-sectional study with chronic cholestasis as study factor and blood levels of vitamin D as outcome. The study included patients aged between 4 months and 18 years, who wer...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2006
Nam Deuk Kim Jeon-Ok Moon Angela L Slitt Bryan L Copple

Hepatocyte injury during cholestasis depends in part on the release of proinflammatory mediators that cause neutrophils to accumulate in the liver and become activated to damage hepatocytes. The mechanism by which cholestasis stimulates production of proinflammatory mediators in the liver is not completely understood. The studies presented here tested the hypothesis that the transcription facto...

Journal: :تحقیقات نظام سلامت 0
فریبا بینش متخصص آسیب شناسی بالینی، دانشکده پزشکی، دانشگاه علوم پزشکی و خدمات بهداشتی درمانی شهید صدوقی یزد. یزد. ایران. مژگان پیری اردکانی دانشجوی دکتری عمومی، دانشکده پزشکی، دانشگاه علوم پزشکی و خدمات بهداشتی درمانی شهید صدوقی یزد. یزد. ایران. (نویسنده مسئول) عزیزالله یوسفی فوق تخصص گوارش کودکان، ، دانشکده پزشکی، دانشگاه علوم پزشکی و خدمات بهداشتی درمانی شهید صدوقی یزد. یزد. ایران.

background: neonatal cholestasis is an important infant’s diseases of liver and biliary, they are wide range of situation including; idiopathic neonatal hepatitis, extrahepatic biliary tract atresia, choledochal cysts and infectious diseases. lack of early diagnosis of the disease can be followed by irreparably complications. the aim of this study was determination the histopathological causes ...

2016
Natalia Gomez-Ospina Carol J. Potter Rui Xiao Kandamurugu Manickam Mi-Sun Kim Kang Ho Kim Benjamin L. Shneider Jennifer L. Picarsic Theodora A. Jacobson Jing Zhang Weimin He Pengfei Liu A. S. Knisely Milton J. Finegold Donna M. Muzny Eric Boerwinkle James R. Lupski Sharon E. Plon Richard A. Gibbs Christine M. Eng Yaping Yang Gabriel C. Washington Matthew H. Porteus William E. Berquist Neeraja Kambham Ravinder J. Singh Fan Xia Gregory M. Enns David D. Moore

Neonatal cholestasis is a potentially life-threatening condition requiring prompt diagnosis. Mutations in several different genes can cause progressive familial intrahepatic cholestasis, but known genes cannot account for all familial cases. Here we report four individuals from two unrelated families with neonatal cholestasis and mutations in NR1H4, which encodes the farnesoid X receptor (FXR),...

2015
Salih Boga Dhanpat Jain Michael L. Schilsky

Progressive familial intrahepatic cholestasis type 3 (PFIC3) is an autosomal recessive disorder of cholestasis of hepatocellular origin, typically seen in infancy or childhood caused by a defect in the ABCB4 located on chromosome 7. Here we report on an older patient, aged 15, who presented with biochemical testing that led to an initial consideration of a diagnosis of Wilson disease (WD) resul...

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