Literature DB >> 28987255

Genetic Testing in Liver Disease: What to Order, in Whom, and When.

Emily A Schonfeld1, Robert S Brown2.   

Abstract

Genetic causes of liver disease lead to a wide range of presentations, from mildly abnormal liver tests to acute liver failure. This article discusses the indications for testing and what to test for hereditary hemochromatosis, progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis, lysosomal acid lipase deficiency, Gilbert syndrome, alpha-1 antitrypsin deficiency, and Wilson disease.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alpha-1 antitrypsin deficiency; Benign recurrent intrahepatic cholestasis; Genetic testing; Gilbert syndrome; Hemochromatosis; Lysosomal acid lipase deficiency; Progressive familial intrahepatic cholestasis; Wilson disease

Mesh:

Year:  2017        PMID: 28987255     DOI: 10.1016/j.cld.2017.06.001

Source DB:  PubMed          Journal:  Clin Liver Dis        ISSN: 1089-3261            Impact factor:   6.126


  2 in total

1.  The Mystery of Episodic Recurrent Jaundice in a Young Male: Cholestasis With a Normal Gamma-Glutamyl Transferase.

Authors:  Samiksha Gupta; Ijlal Akbar Ali; Eleanor Abreo; Veena Gujju; Maham Hayat
Journal:  Cureus       Date:  2021-03-11

2.  Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children.

Authors:  Xinshuo Lu; Simin Li; Wen Zhang; Yunting Lin; Zhikun Lu; Yanna Cai; Xueying Su; Yongxian Shao; Zongcai Liu; Huiying Sheng; Yonglan Huang; Li Liu; Chunhua Zeng
Journal:  BMC Gastroenterol       Date:  2022-03-16       Impact factor: 3.067

  2 in total

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