A Rare Cause of Neonatal Cholestasis Without Liver Dysfunction
نویسندگان
چکیده
منابع مشابه
Arthrogryposis-renal tubular dysfunction-cholestasis syndrome: a cause of neonatal cholestasis. Case report.
Arthrogryposis-renal dysfunction-cholestasis syndrome is a rare lethal disorder that involves multipl organ system. It is inherited autosomal recessive and caused by defects in the VPS33B and VIPAR genes. Three cardinal findings of this syndrome are arthrogryposis, renal tubular dysfunction and cholestasis.The other organ involvements including ichthyosis, central nervous system malformation, p...
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We report a case of a newborn with cholestasis that was diagnosed as nonsyndromic Alagille syndrome. The main feature of the disease is a paucity of biliary ducts. There are two known types of the disease: the syndromic type which is associated with other congenital defects and the nonsyndromic type without other anomalies detected at birth. We describe the case and discuss its clinical and rad...
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2. García Gallego F, Gamallo Amat C, Aguado MG. Registro Nacional de tumores (memoria 1996-1997). Rev Esp Cardiol. 1999;52:13-20. 3. Burke A, Jeudy J Jr, Virmani R. Cardiac tumors: An update. Heart. 2008;94;117-23. 4. Neragi-Miandoab S, Kim J, Vlahakes GJ. Malignant tumors of the heart: a review of tumor type, dianosis and therapy. Clin Oncol (R Coll Radiol). 2007;19:748-56. 5. Constatine G, Sh...
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ژورنال
عنوان ژورنال: Gastroenterology
سال: 2019
ISSN: 0016-5085
DOI: 10.1053/j.gastro.2019.01.031