Literature DB >> 29502911

Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders.

Marshall L Summar1, Nicholas Ah Mew2.   

Abstract

The urea cycle disorders are a group of inherited biochemical diseases caused by a complete or partial deficiency of any one of the enzymes or transport proteins required to convert toxic ammonia into urea and to produce arginine and citrulline. The clinical manifestations of these disorders are mostly the result of acute or chronic hyperammonemia, which affects the central nervous system. Affected individuals can also develop hepatic dysfunction. These disorders can present at any age from the immediate newborn to later in life. Early diagnosis and treatment are key to improving outcomes.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ammonia; Arginine; Citrulline; Hyperammonemia; Liver; Ornithine; Urea cycle

Mesh:

Substances:

Year:  2018        PMID: 29502911     DOI: 10.1016/j.pcl.2017.11.004

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


  16 in total

1.  Peripheral venous route for administration of ammonul infusion for treatment of acute hyperammonemia. An experience from a tertiary center in Saudi Arabia.

Authors:  Amal M Alhashem; Rihab M Salih; Aida I Al-Aqeel; Sarar Mohamed
Journal:  Saudi Med J       Date:  2020-01       Impact factor: 1.484

Review 2.  Hyperammonemia in Inherited Metabolic Diseases.

Authors:  Graziela Schmitt Ribas; Franciele Fátima Lopes; Marion Deon; Carmen Regla Vargas
Journal:  Cell Mol Neurobiol       Date:  2021-10-19       Impact factor: 4.231

3.  Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism.

Authors:  Alba-Aina Castells; Daniela Gueraldi; Rafel Balada; Alba Tristán-Noguero; Elisenda Cortès-Saladelafont; Federico Ramos; Silvia Meavilla; Mariela De Los Santos; Camila Garcia-Volpe; Roser Colomé; Maria Luz Couce; Cristina Sierra; Aida Ormazábal; Marta Batllori; Rafael Artuch; Judith Armstrong; Soledad Alcántara; Àngels Garcia-Cazorla
Journal:  Sci Rep       Date:  2019-06-24       Impact factor: 4.379

4.  Metabolomic Profiling of Cerebral Palsy Brain Tissue Reveals Novel Central Biomarkers and Biochemical Pathways Associated with the Disease: A Pilot Study.

Authors:  Zeynep Alpay Savasan; Ali Yilmaz; Zafer Ugur; Buket Aydas; Ray O Bahado-Singh; Stewart F Graham
Journal:  Metabolites       Date:  2019-02-02

5.  Molecular, biochemical, and clinical analyses of five patients with carbamoyl phosphate synthetase 1 deficiency.

Authors:  Lijuan Fan; Jing Zhao; Li Jiang; Lingling Xie; Jiannan Ma; Xiujuan Li; Min Cheng
Journal:  J Clin Lab Anal       Date:  2019-11-20       Impact factor: 2.352

Review 6.  Neuropsychological attributes of urea cycle disorders: A systematic review of the literature.

Authors:  Susan E Waisbren; Arianna K Stefanatos; Teresa M Y Kok; Burcu Ozturk-Hismi
Journal:  J Inherit Metab Dis       Date:  2019-08-01       Impact factor: 4.982

7.  Early care of N-acetyl glutamate synthase (NAGS) deficiency in three infants from an inbred family.

Authors:  Katell Peoc'h; Léna Damaj; Romain Pelletier; Charles Lefèvre; Christèle Dubourg; Marie-Christine Denis; Claude Bendavid; Sylvie Odent; Caroline Moreau
Journal:  Mol Genet Metab Rep       Date:  2020-01-24

8.  Diagnostics of Inherited Metabolic Diseases in Newborns with the Hyperammonemia Syndrome at the Onset of Disease (Pilot Study).

Authors:  A N Kolchina; E E Yatsyshina; L V Malysheva; E E Ledentsova; E E Lidyaeva; O V Khaletskaya
Journal:  Sovrem Tekhnologii Med       Date:  2021-02-28

Review 9.  Recent advances in understanding liver fibrosis: bridging basic science and individualized treatment concepts.

Authors:  Ralf Weiskirchen; Sabine Weiskirchen; Frank Tacke
Journal:  F1000Res       Date:  2018-06-27

Review 10.  A Great Catch for Investigating Inborn Errors of Metabolism-Insights Obtained from Zebrafish.

Authors:  Maximilian Breuer; Shunmoogum A Patten
Journal:  Biomolecules       Date:  2020-09-22
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