Literature DB >> 28502442

Neonatal Cholestasis.

Erin Lane1, Karen F Murray2.   

Abstract

Neonatal jaundice is common and usually not concerning when it is secondary to unconjugated hyperbilirubinemia, below the neurotoxic level, and resolves early. Primary care providers should be vigilant, however, about evaluating infants in whom jaundice presents early, is prolonged beyond 2 weeks of life, or presents at high levels. Even in well-appearing infants, fractionated (direct and indirect) bilirubin levels should be obtained in these clinical scenarios to evaluate for potential cholestasis. This review presents an approach to the evaluation of a jaundiced infant and discusses diagnosis and management of several causes of neonatal cholestasis.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biliary atresia; Cholestasis; Jaundice; Neonatal cholestasis; Neonatal liver disease

Mesh:

Substances:

Year:  2017        PMID: 28502442     DOI: 10.1016/j.pcl.2017.01.006

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  9 in total

1.  Comprehensive Analysis of Gut Microbiota and Fecal Bile Acid Profiles in Children With Biliary Atresia.

Authors:  Ting Yang; Shen Yang; Jiawei Zhao; Peize Wang; Siqi Li; Yuyan Jin; Zhaozhou Liu; Xinyue Zhang; Yanan Zhang; Yong Zhao; Junmin Liao; Shuangshuang Li; Kaiyun Hua; Yichao Gu; Dingding Wang; Jinshi Huang
Journal:  Front Cell Infect Microbiol       Date:  2022-06-17       Impact factor: 6.073

Review 2.  Biliary atresia and congenital disorders of the extrahepatic bile ducts.

Authors:  Ali Islek; Gokhan Tumgor
Journal:  World J Gastrointest Pharmacol Ther       Date:  2022-07-05

Review 3.  Recent developments in diagnostics and treatment of neonatal cholestasis.

Authors:  Amy G Feldman; Ronald J Sokol
Journal:  Semin Pediatr Surg       Date:  2020-07-23       Impact factor: 2.754

4.  A case report of a challenging diagnosis of biliary atresia in a patient receiving total parenteral nutrition.

Authors:  Atu Agawu; Andrew Wehrman; Jennifer Pogoriler; Natalie A Terry; Henry C Lin
Journal:  BMC Pediatr       Date:  2019-03-08       Impact factor: 2.125

Review 5.  Newer variants of progressive familial intrahepatic cholestasis.

Authors:  Vignesh Vinayagamoorthy; Anshu Srivastava; Moinak Sen Sarma
Journal:  World J Hepatol       Date:  2021-12-27

6.  Association of Gut Microbiota and Metabolites With Disease Progression in Children With Biliary Atresia.

Authors:  Wei Song; Li-Ying Sun; Zhi-Jun Zhu; Lin Wei; Wei Qu; Zhi-Gui Zeng; Ying Liu; Hai-Ming Zhang; Wei Guo
Journal:  Front Immunol       Date:  2021-09-23       Impact factor: 7.561

7.  A Two-Year Clinical Description of a Patient with a Rare Type of Low-GGT Cholestasis Caused by a Novel Variant of USP53.

Authors:  Olga Shatokhina; Natalia Semenova; Nina Demina; Elena Dadali; Alexander Polyakov; Oxana Ryzhkova
Journal:  Genes (Basel)       Date:  2021-10-14       Impact factor: 4.096

8.  Etiology of neonatal cholestasis after emerging molecular diagnostics.

Authors:  Huanhuan Wang; Lin Yang; Jin Wang
Journal:  Transl Pediatr       Date:  2022-03

9.  Ursodeoxycholic Acid and SMOFlipid for Treating Parenteral Nutrition Associated Cholestasis in Infants.

Authors:  Saleh Al-Alaiyan; Weam Elsaidawi; Amal M Alanazi; Raef A Qeretli; Najlaa A Abdulaziz; Areej Alfattani
Journal:  Cureus       Date:  2022-02-09
  9 in total

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