Literature DB >> 22610979

A rare case of hyperammonemia complication of high-protein parenteral nutrition.

Unnikrishnan Pillai1, Roopkiranjot Kahlon, James Sondheimer, Pravit Cadnapaphorncai, Zeenat Bhat.   

Abstract

Hyperammonemia is a metabolic derangement that can be potentially fatal. Primary hyperammonemia due to urea cycle enzyme deficiency is usually discovered in neonates but rarely can present in adulthood. Late-onset manifestations of urea cycle disorders can go unnoticed, until they become life threatening. The authors report a 28-year-old man who developed hyperammonemia in the hospital following parenteral nutrition (PN), leading to cerebral edema, which was fatal despite resolution of the hyperammonemia with cessation of PN and the use of continuous renal replacement therapy.

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Year:  2012        PMID: 22610979     DOI: 10.1177/0148607112447815

Source DB:  PubMed          Journal:  JPEN J Parenter Enteral Nutr        ISSN: 0148-6071            Impact factor:   4.016


  6 in total

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Journal:  Nat Med       Date:  2013-12       Impact factor: 53.440

2.  Features of Adult Hyperammonemia Not Due to Liver Failure in the ICU.

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Journal:  Crit Care Med       Date:  2018-09       Impact factor: 7.598

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Journal:  Anal Biochem       Date:  2021-10-09       Impact factor: 3.365

Review 4.  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

5.  Psychiatric adult-onset of urea cycle disorders: A case-series.

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Journal:  Mol Genet Metab Rep       Date:  2017-07-06

Review 6.  Management of late onset urea cycle disorders-a remaining challenge for the intensivist?

Authors:  S Redant; A Empain; A Mugisha; P Kamgang; R Attou; P M Honoré; D De Bels
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  6 in total

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