Literature DB >> 24495602

Liver transplantation for pediatric metabolic disease.

George Mazariegos1, Benjamin Shneider2, Barbara Burton3, Ira J Fox4, Nedim Hadzic5, Priya Kishnani6, D Holmes Morton7, Sara McIntire8, Ronald J Sokol9, Marshall Summar10, Desiree White11, Vincent Chavanon12, Jerry Vockley13.   

Abstract

Liver transplantation (LTx) was initially developed as a therapy for liver diseases known to be associated with a high risk of near-term mortality but is based upon a different set of paradigms for inborn metabolic diseases. As overall outcomes for the procedure have improved, LTx has evolved into an attractive approach for a growing number of metabolic diseases in a variety of clinical situations. No longer simply life-saving, the procedure can lead to a better quality of life even if not all symptoms of the primary disorder are eliminated. Juggling the risk-benefit ratio thus has become more complicated as the list of potential disorders amenable to treatment with LTx has increased. This review summarizes presentations from a recent conference on metabolic liver transplantation held at the Children's Hospital of Pittsburgh of UPMC on the role of liver or hepatocyte transplantation in the treatment of metabolic liver disease.
Copyright © 2014. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amino aciduria; Hepatocyte transplant; Inborn errors of metabolism; Liver failure; Liver transplant; Organic acidemia

Mesh:

Year:  2014        PMID: 24495602     DOI: 10.1016/j.ymgme.2014.01.006

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  19 in total

1.  New Tools in Experimental Cellular Therapy for the Treatment of Liver Diseases.

Authors:  Jennifer R Ferrer; Attasit Chokechanachaisakul; Jason A Wertheim
Journal:  Curr Transplant Rep       Date:  2015-06-01

Review 2.  Role of liver progenitors in liver regeneration.

Authors:  Jan Best; Paul Manka; Wing-Kin Syn; Laurent Dollé; Leo A van Grunsven; Ali Canbay
Journal:  Hepatobiliary Surg Nutr       Date:  2015-02       Impact factor: 7.293

Review 3.  Recent advances in liver transplantation for metabolic disease.

Authors:  P J Mc Kiernan
Journal:  J Inherit Metab Dis       Date:  2017-02-06       Impact factor: 4.982

4.  Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs.

Authors:  Víctor R De Jesús; Barbara W Adam; Daniel Mandel; Carla D Cuthbert; Dietrich Matern
Journal:  Mol Genet Metab       Date:  2014-07-17       Impact factor: 4.797

5.  Hepatocyte Transplantation.

Authors:  Ira J Fox
Journal:  Gastroenterol Hepatol (N Y)       Date:  2014-09

Review 6.  Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Authors:  Kimihiko Oishi; Ronen Arnon; Melissa P Wasserstein; George A Diaz
Journal:  Pediatr Transplant       Date:  2016-06-21

7.  PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?

Authors:  D Coman; P Lewindon; P Clayton; K Riney
Journal:  JIMD Rep       Date:  2015-06-25

Review 8.  Metabolic Liver Disease: When to Suspect and How to Diagnose?

Authors:  Seema Alam; Vikrant Sood
Journal:  Indian J Pediatr       Date:  2016-04-29       Impact factor: 1.967

9.  Efficacy of Living Donor Liver Transplantation in Patients with Methylmalonic Acidemia.

Authors:  Jae Guk Jang; Seak Hee Oh; Yu Bin Kim; Seo Hee Kim; Han-Wook Yoo; Beom Hee Lee; Jung-Man Namgoong; Dae Yeon Kim; Ki-Hun Kim; Gi-Won Song; Deok-Bog Moon; Shin Hwang; Sung-Gyu Lee; Kyung Mo Kim
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2021-05-04

10.  Liver transplantation in children with inborn errors of metabolism: 30 years experience in NSW, Australia.

Authors:  Noha Elserafy; Sue Thompson; Troy Dalkeith; Michael Stormon; Gordon Thomas; Albert Shun; Janine Sawyer; Shanti Balasubramanian; Kaustuv Bhattacharya; Nadia Badawi; Carolyn Ellaway
Journal:  JIMD Rep       Date:  2021-05-04
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.