Breningstall G N
Department of Pediatrics, Temple University School of Medicine, Philadelphia, Pennsylvania.
Pediatr Neurol. 1986 Sep-Oct;2(5):253-62. doi: 10.1016/0887-8994(86)90016-0.
This article reviews the neurologic manifestations of hyperammonemic disorders. A variety of inborn errors of metabolism, as well as transient neonatal or acquired hepatic dysfunctions, are identified as causes of hyperammonemia. The pathogenesis of hyperammonemia in these disorders is outlined. Catastrophic hyperammonemia and hyperammonemic coma are described; algorithms to establish specific diagnosis are suggested. Symptoms of less severe ammonia intoxication, which also occur in more common diseases, are described. The need to consider hyperammonemia as a potential etiology for these symptoms is emphasized. Finally, the neurotoxicity of ammonia is discussed.
本文综述了高氨血症性疾病的神经系统表现。多种先天性代谢缺陷以及短暂性新生儿或获得性肝功能障碍被确定为高氨血症的病因。概述了这些疾病中高氨血症的发病机制。描述了暴发性高氨血症和高氨血症性昏迷;提出了建立特异性诊断的流程。还描述了在更常见疾病中也会出现的不太严重的氨中毒症状。强调了将高氨血症视为这些症状潜在病因的必要性。最后,讨论了氨的神经毒性。