Cranial MRI in Acute Hyperammonemic Encephalopathy

被引：25
|
作者：
Bindu, Parayil S. [1 ]
Sinha, Sanjib [1 ]
Taly, Arun B. [1 ]
Christopher, Rita [2 ]
Kovoor, Jerry M. E. [3 ]
机构：
[1] Natl Inst Mental Hlth & Neurosci, Dept Neurol, Bangalore 560029, Karnataka, India
[2] Natl Inst Mental Hlth & Neurosci, Dept Neurochem, Bangalore 560029, Karnataka, India
[3] Natl Inst Mental Hlth & Neurosci, Dept Neuroimaging & Intervent Radiol, Bangalore 560029, Karnataka, India
来源：
PEDIATRIC NEUROLOGY | 2009年 / 41卷 / 02期
关键词：
ORNITHINE TRANSCARBAMYLASE DEFICIENCY; UREA CYCLE DISORDERS; CITRULLINEMIA;
D O I：
10.1016/j.pediatrneurol.2009.02.012
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
Cranial magnetic resonance imaging was performed in three cases of acute hyperammonemic encephalopathy with three diverse etiologies: infantile citrullinemia, acute hepatic encephalopathy, and proximal urea cycle disorder. All three patients exhibited diffuse extensive cortical signal changes and swelling. Neurologic outcome was poor in all three cases. Knowledge of the magnetic resonance imaging findings of hyperammonemic encephalopathy may help in early diagnosis and treatment and could influence the neurologic outcome. (C) 2009 by Elsevier Inc. All rights reserved.
引用
收藏
页码：139 / 142
页数：4
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