Literature DB >> 7666324

Orthotopic liver transplantation for ornithine transcarbamylase deficiency with hyperammonemic encephalopathy.

T Hasegawa1, A G Tzakis, S Todo, J Reyes, B Nour, D N Finegold, T E Starzl.   

Abstract

Ornithine transcarbamylase (OTC) deficiency is an X chromosome-linked disorder causing hyperammonemic encephalopathy with a very poor prognosis. We describe here two patients with OTC deficiency, one a late on-set female patient (case 1) and the other a neonatal-onset male patient (case 2), who were successfully treated with orthotopic liver transplantation (OLTx). The OTC activity in the excised liver was 10% and 0% of control, respectively. Hyperammonemic encephalopathy was controlled with medical therapy in case 1 until the of 5 years, but the complicated course in case 2 in which hyperammonemia required peritoneal dialysis and hemodialysis in the neonatal period necessitated OLTx with a reduced-size liver at the age of 80 days. Both patients had restoration of serum ammonia level to normal in 2 and 3 days after liver replacement, and both patients have normal neurological and developmental status after 2 and 0.5 years of postoperative follow-up. These cases illustrate not only the metabolic cure of this disorder, but also the need to preserve neurological integrity by aggressive medical management of the hyperammonemia preoperatively and early surgical intervention when indicated, even if this is required very early in life.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7666324      PMCID: PMC2975439          DOI: 10.1016/0022-3468(95)90766-1

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  10 in total

Review 1.  The clinical, biochemical, and molecular spectrum of ornithine transcarbamylase deficiency.

Authors:  M Tuchman
Journal:  J Lab Clin Med       Date:  1992-12

2.  Orthotopic liver transplantation with preservation of the inferior vena cava.

Authors:  A Tzakis; S Todo; T E Starzl
Journal:  Ann Surg       Date:  1989-11       Impact factor: 12.969

3.  Prospective treatment of urea cycle disorders.

Authors:  N E Maestri; E R Hauser; D Bartholomew; S W Brusilow
Journal:  J Pediatr       Date:  1991-12       Impact factor: 4.406

4.  Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency.

Authors:  J E Spence; A Maddalena; W E O'Brien; S D Fernbach; M L Batshaw; C O Leonard; A L Beaudet
Journal:  J Pediatr       Date:  1989-04       Impact factor: 4.406

5.  Liver transplantation for ornithine transcarbamylase deficiency in a girl.

Authors:  C Largillière; D Houssin; F Gottrand; C Mathey; A Checoury; D Alagille; J P Farriaux
Journal:  J Pediatr       Date:  1989-09       Impact factor: 4.406

6.  Ornithine transcarbamylase deficiency: neuropathologic changes acquired in utero.

Authors:  F Filloux; J J Townsend; C Leonard
Journal:  J Pediatr       Date:  1986-06       Impact factor: 4.406

7.  Application of reduced-size liver transplants as split grafts, auxiliary orthotopic grafts, and living related segmental transplants.

Authors:  C E Broelsch; J C Emond; P F Whitington; J R Thistlethwaite; A L Baker; J L Lichtor
Journal:  Ann Surg       Date:  1990-09       Impact factor: 12.969

8.  Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.

Authors:  S W Brusilow; M Danney; L J Waber; M Batshaw; B Burton; L Levitsky; K Roth; C McKeethren; J Ward
Journal:  N Engl J Med       Date:  1984-06-21       Impact factor: 91.245

9.  Orthotopic liver transplantation for urea cycle enzyme deficiency.

Authors:  S Todo; T E Starzl; A Tzakis; K J Benkov; F Kalousek; T Saheki; K Tanikawa; W A Fenton
Journal:  Hepatology       Date:  1992-03       Impact factor: 17.425

10.  Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.

Authors:  M Msall; M L Batshaw; R Suss; S W Brusilow; E D Mellits
Journal:  N Engl J Med       Date:  1984-06-07       Impact factor: 91.245

  10 in total
  5 in total

Review 1.  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

2.  Early orthotopic liver transplantation in urea cycle defects: follow up of a developmental outcome study.

Authors:  Philippe M Campeau; Penelope J Pivalizza; Geoffrey Miller; Kim McBride; Saul Karpen; John Goss; Brendan H Lee
Journal:  Mol Genet Metab       Date:  2010-02-19       Impact factor: 4.797

3.  Liver transplantation for the treatment of urea cycle disorders.

Authors:  P F Whitington; E M Alonso; J T Boyle; J P Molleston; P Rosenthal; J C Emond; J M Millis
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982

4.  Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene.

Authors:  Ernie Zuraida Ali; Yuslina Zakaria; Mohd Amran Mohd Radzi; Lock Hock Ngu; Siti Azma Jusoh
Journal:  Biomed Res Int       Date:  2018-08-05       Impact factor: 3.411

Review 5.  Liver transplantation in rare late-onset ornithine transcarbamylase deficiency with central nervous system injury: A case report and review of the literature.

Authors:  Xin Jin; Xinchen Zeng; Dong Zhao; Nan Jiang
Journal:  Brain Behav       Date:  2022-09-20       Impact factor: 3.405

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.