精氨酸酶
尿素循环
医学
高氨血症
脑病
痉挛性双瘫
内科学
儿科
内分泌学
精氨酸
生物化学
精神科
脑瘫
生物
氨基酸
作者
LeemaPauline Cornelius,Vivekasaravanan Raju,Asir Julin
标识
DOI:10.4103/jpn.jpn_36_19
摘要
Urea cycle disorders are rare metabolic disorders that present as encephalopathy with hyperammonemia. Arginase deficiency causing hyperargininemia is one among the urea cycle disorders, which usually presents as spastic diplegia. Hyperammonemic encephalopathy is rare in arginase deficiency. We present a rare case of arginase deficiency presenting as acute encephalopathy in a child.
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