Zobrazeno 1 - 10
of 369
pro vyhledávání: '"Indian childhood cirrhosis"'
Autor:
Moinak Sen Sarma, Jayendra Seetharaman
Publikováno v:
World Journal of Hepatology
Chelation is the mainstay of therapy in certain pediatric liver diseases. Copper and iron related disorders require chelation. Wilson’s disease (WD), one of the common causes of cirrhosis in children is treated primarily with copper chelating agent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba2ce8b562acaafef9de06be523d519e
https://doi.org/10.4254/wjh.v13.i11.1552
https://doi.org/10.4254/wjh.v13.i11.1552
Akademický článek
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Akademický článek
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Autor:
Carmen Espinós, Peter Ferenci
Publikováno v:
JHEP Reports
Summary The diagnosis of Wilson disease is not always easy. For many patients, a combination of tests reflecting disturbed copper metabolism may be needed. Testing for ATP7B variants has become part of the routine diagnostic approach. The methods of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39396ae01056eccafde511e7472b40a1
http://europepmc.org/articles/PMC7322184
http://europepmc.org/articles/PMC7322184
Autor:
Srinivas Sankaranarayanan, Rakesh Manoharan, Sivanandam Sundaram, Valavanur Subramanian Sankaranarayanan, Mukul Vij
Publikováno v:
J Clin Exp Hepatol
Cholestatic jaundice in new born and infants results from biliary obstruction or hepatocellular dysfunction. Biliary atresia (BA) and Idiopathic neonatal hepatitis comprises the major aetiology. Cholestasis due to toxins is rare in infants. Indian ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25a74c7defdbed6403affac14cb909fe
https://doi.org/10.1016/j.jceh.2021.07.006
https://doi.org/10.1016/j.jceh.2021.07.006
Akademický článek
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Publikováno v:
Journal of clinical pathology. 74(11)
This case describes a 15-month boy with a 6-month history suggestive of liver disease. His similarly affected non-identical twin died and autopsy investigations were consistent with intrahepatic cholestasis, progressive liver damage complicated by ci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03110b796d3d24d8519f2f27260621a
https://pubmed.ncbi.nlm.nih.gov/34321224
https://pubmed.ncbi.nlm.nih.gov/34321224
Autor:
Aarti Behera, Mangal Charan Murmu
Publikováno v:
Pediatric Review: International Journal of Pediatric Research. 5:31-36
Introduction: Chronic liver diseases(CLD) account for 1 to 5% of paediatric ward admissions and upto 20% of ward mortality in our country. Now a day Indian childhood cirrhosis is a rarity, whereas diseases likechronic hepatitis, Wilsons disease and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf3ebc5d7a09c3a06df57359020019d0
https://doi.org/10.17511/ijpr.2018.i01.07
https://doi.org/10.17511/ijpr.2018.i01.07
Publikováno v:
Journal of Postgraduate Medicine, Vol 64, Iss 2, Pp 104-108 (2018)
Journal of Postgraduate Medicine
Journal of Postgraduate Medicine
Indian childhood cirrhosis is an entity believed to be on the verge of extinction. We present the case of a 13-month-old girl presenting acutely with jaundice, fever, and persistently increasing bilirubin. Investigations revealed direct hyperbilirubi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0bd79c57164bcc3c66181d512164ea5
http://www.jpgmonline.com/article.asp?issn=0022-3859
http://www.jpgmonline.com/article.asp?issn=0022-3859
Autor:
Massimiliano Paganelli, Fernando Alvarez, L Khendek, E Drouin, Michel Lallier, Mona Beaunoyer
Publikováno v:
Journal of the Canadian Association of Gastroenterology. 4:252-253
Background North American Indian Childhood Cirrhosis (NAIC) has only been described in the Cree-Ojibway First Nations of Northern Quebec. NAIC presents with transient neonatal jaundice and progresses to biliary cirrhosis often requiring liver transpl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c12ce643778ad4aa31d58d677200441
https://doi.org/10.1093/jcag/gwab002.217
https://doi.org/10.1093/jcag/gwab002.217