Hyperammonemia in review: pathophysiology, diagnosis, and treatment

被引:0
|
作者
Ari Auron
Patrick D. Brophy
机构
[1] Blank Memorial Hospital for Children,Department of Pediatrics, Pediatric Nephrology, Dialysis & transplantation
[2] University of Iowa Children’s Hospital,undefined
来源
Pediatric Nephrology | 2012年 / 27卷
关键词
Hyperammonemia; Dialysis; Urea cycle defects; Treatment; Pathophysiology;
D O I
暂无
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学科分类号
摘要
Ammonia is an important source of nitrogen and is required for amino acid synthesis. It is also necessary for normal acid-base balance. When present in high concentrations, ammonia is toxic. Endogenous ammonia intoxication can occur when there is impaired capacity of the body to excrete nitrogenous waste, as seen with congenital enzymatic deficiencies. A variety of environmental causes and medications may also lead to ammonia toxicity. Hyperammonemia refers to a clinical condition associated with elevated ammonia levels manifested by a variety of symptoms and signs, including significant central nervous system (CNS) abnormalities. Appropriate and timely management requires a solid understanding of the fundamental pathophysiology, differential diagnosis, and treatment approaches available. The following review discusses the etiology, pathogenesis, differential diagnosis, and treatment of hyperammonemia.
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页码:207 / 222
页数:15
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