Literature DB >> 33369132

Acute liver dysfunction with delayed peak of serum aminotransferase levels as a presentation of ornithine transcarbamylase deficiency in females.

Kathryn Clarkston1,2, Joy Lee3,4, Sarah Donoghue4, Heidi Peters3,4, Hernan Eiroa5, Amit A Shah6,7, Kathleen Loomes6,7, Jessica Wen6,7, Mark Oliver3,8, Winita Hardikar3,8, Carlos E Prada1,9, Akihiro Asai1,2.   

Abstract

We describe 10 females with ornithine transcarbamylase (OTC) deficiency and liver dysfunction, revealing a unique pattern of hepatocyte injury in which initial hyperammonemia and coagulopathy is followed by a delayed peak in aminotransferase levels. None of the patients required urgent liver transplantation, though five eventually underwent transplant for recurrent metabolic crises. We intend that this novel observation will initiate further investigations into the pathophysiology of liver dysfunction in OTC-deficient patients, and ultimately lead to the development of therapies and prevent the need for liver transplant.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  acute liver dysfunction; female manifestation of OTC deficiency; hepatic lyonization; hyperammonemia; ornithine transcarbamylase

Mesh:

Substances:

Year:  2020        PMID: 33369132      PMCID: PMC7974766          DOI: 10.1002/ajmg.a.62031

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  15 in total

1.  Hyperammonaemia due to ornithine transcarbamylase deficiency.

Authors:  I J Hopkins; J F Connelly; A G Dawson; F J Hird; T G Maddison
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

2.  Inherited metabolic disorders presenting as acute liver failure in newborns and young children: King's College Hospital experience.

Authors:  Robert Hegarty; Nedim Hadzic; Paul Gissen; Anil Dhawan
Journal:  Eur J Pediatr       Date:  2015-04-24       Impact factor: 3.183

3.  Variable X-chromosome inactivation and enlargement of pericentral glutamine synthetase zones in the liver of heterozygous females with OTC deficiency.

Authors:  Dita Musalkova; Eva Sticova; Martin Reboun; Jitka Sokolova; Jakub Krijt; Jitka Honzikova; Jiri Gurka; Magdalena Neroldova; Tomas Honzik; Jiri Zeman; Milan Jirsa; Lenka Dvorakova; Martin Hrebicek
Journal:  Virchows Arch       Date:  2018-04-06       Impact factor: 4.064

4.  High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure.

Authors:  Ulrike Teufel; Jürgen Weitz; Christa Flechtenmacher; Viola Prietsch; Jan Schmidt; Georg F Hoffmann; Stefan Kölker; Guido Engelmann
Journal:  Pediatr Transplant       Date:  2009-04-26

5.  Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.

Authors:  Renata C Gallagher; Christina Lam; Derek Wong; Stephen Cederbaum; Ronald J Sokol
Journal:  J Pediatr       Date:  2014-01-30       Impact factor: 4.406

6.  EASL Clinical Practical Guidelines on the management of acute (fulminant) liver failure.

Authors:  Julia Wendon,; Juan Cordoba; Anil Dhawan; Fin Stolze Larsen; Michael Manns; Didier Samuel; Kenneth J Simpson; Ilan Yaron; Mauro Bernardi
Journal:  J Hepatol       Date:  2017-05       Impact factor: 25.083

Review 7.  Liver involvement in urea cycle disorders: a review of the literature.

Authors:  Adrien Bigot; Michel C Tchan; Benjamin Thoreau; Hélène Blasco; François Maillot
Journal:  J Inherit Metab Dis       Date:  2017-09-12       Impact factor: 4.982

8.  Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiency.

Authors:  E Zammarchi; M A Donati; L Filippi; M Resti
Journal:  J Pediatr Gastroenterol Nutr       Date:  1996-05       Impact factor: 2.839

9.  Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.

Authors:  Jiandi Gao; Feng Gao; Fang Hong; Huimin Yu; Peifang Jiang
Journal:  Am J Emerg Med       Date:  2014-08-23       Impact factor: 2.469

10.  Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD).

Authors:  Alexander Laemmle; Renata C Gallagher; Adrian Keogh; Tamar Stricker; Matthias Gautschi; Jean-Marc Nuoffer; Matthias R Baumgartner; Johannes Häberle
Journal:  PLoS One       Date:  2016-04-12       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.