Literature DB >> 19343772

Ornithine transcarbamylase deficiency: a possible risk factor for thrombosis.

Lakshmi Venkateswaran1, Fernando Scaglia, Valerie McLin, Paula Hertel, Oleg A Shchelochkov, Saul Karpen, Donald Mahoney, Donald L Yee.   

Abstract

Ornithine transcarbamylase (OTC) deficiency is the most common urea cycle defect. Thromboembolic complications have not heretofore been linked with this diagnosis. We describe four patients with neonatal-onset OTC deficiency who developed vascular thromboses. One patient had arterial thrombosis; the rest developed venous thromboses. Multiple pro-thrombotic risk factors were identified. Low plasma arginine levels were observed in all patients at the time of thrombosis. Arginine deficiency and the resultant nitric oxide insufficiency may contribute to thrombotic risk. Careful normalization of plasma arginine and citrulline levels and increased surveillance for thrombotic complications should be considered in patients with OTC deficiency. Copyright 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19343772      PMCID: PMC4869977          DOI: 10.1002/pbc.22016

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  11 in total

Review 1.  Ornithine carbamoyltransferase deficiency.

Authors:  J E Wraith
Journal:  Arch Dis Child       Date:  2001-01       Impact factor: 3.791

Review 2.  Nitric oxide insufficiency, platelet activation, and arterial thrombosis.

Authors:  J Loscalzo
Journal:  Circ Res       Date:  2001-04-27       Impact factor: 17.367

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Authors:  Reinhard Schneppenheim; Jeanette Greiner
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2006

Review 5.  Current role of liver transplantation for the treatment of urea cycle disorders: a review of the worldwide English literature and 13 cases at Kyoto University.

Authors:  Daisuke Morioka; Mureo Kasahara; Yasutsugu Takada; Yasumasa Shirouzu; Kaoru Taira; Seisuke Sakamoto; Kenji Uryuhara; Hiroto Egawa; Hiroshi Shimada; Koichi Tanaka
Journal:  Liver Transpl       Date:  2005-11       Impact factor: 5.799

Review 6.  The many antithrombotic actions of nitric oxide.

Authors:  Constantine Tziros; Jane E Freedman
Journal:  Curr Drug Targets       Date:  2006-10       Impact factor: 3.465

7.  Development of the human coagulation system in the full-term infant.

Authors:  M Andrew; B Paes; R Milner; M Johnston; L Mitchell; D M Tollefsen; P Powers
Journal:  Blood       Date:  1987-07       Impact factor: 22.113

Review 8.  New functional aspects of the L-arginine-nitric oxide metabolism within the circulating blood.

Authors:  Petra Kleinbongard; Stefanie Keymel; Malte Kelm
Journal:  Thromb Haemost       Date:  2007-11       Impact factor: 5.249

Review 9.  Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism.

Authors:  Fernando Scaglia; Nicola Brunetti-Pierri; Soledad Kleppe; Juan Marini; Susan Carter; Peter Garlick; Farook Jahoor; William O'Brien; Brendan Lee
Journal:  J Nutr       Date:  2004-10       Impact factor: 4.798

10.  Evidence for the presence of L-arginine-nitric oxide pathway in human red blood cells: relevance in the effects of red blood cells on platelet function.

Authors:  L Y Chen; J L Mehta
Journal:  J Cardiovasc Pharmacol       Date:  1998-07       Impact factor: 3.105

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  4 in total

1.  Two novel mutations of ornithine transcarbamylase gene identified from three Chinese neonates with ornithine transcarbamylase deficiency.

Authors:  Jing Liu; Lei Dong; Yan Wang; Mei Zhang
Journal:  Int J Clin Exp Med       Date:  2015-02-15

2.  Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency.

Authors:  Peter N Eskander; Sara S Romani
Journal:  Cureus       Date:  2021-11-30

Review 3.  Hyperammonemia due to urea cycle disorders: a potentially fatal condition in the intensive care setting.

Authors:  Marcel Cerqueira Cesar Machado; Fabiano Pinheiro da Silva
Journal:  J Intensive Care       Date:  2014-03-13

4.  SARS CoV2 infection in a young subject affected by arginosuccinate synthase deficiency: A case report of epilepsy worsening.

Authors:  N Vitturi; L Lenzini; F Francini-Pesenti; G Gugelmo; A Avogaro
Journal:  Mol Genet Metab Rep       Date:  2020-12-11
  4 in total

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