An autopsy case of ornithine transcarbamylase deficiency

被引:16
作者
Yamanouchi, H
Yokoo, H
Yuhara, Y
Maruyama, K
Sasaki, A
Hirato, J
Nakazato, Y
机构
[1] Dokkyo Univ, Sch Med, Dept Pediat, Pediat Neurol Grp, Mibu, Tochigi 3210293, Japan
[2] Gunma Univ, Sch Med, Dept Pathol 1, Maebashi, Gumma 371, Japan
[3] Gunma Childrens Med Ctr, Dept Pediat, Seta, Gunma, Japan
[4] Gunma Childrens Med Ctr, Dept Neonatol, Seta, Gunma, Japan
关键词
ornithine transcarbamylase deficiency; grumose degeneration; dentate nucleus; multicystic encephalopathy;
D O I
10.1016/S0387-7604(01)00408-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We present an autopsy case of ornithine transcarbamylase (OTC) deficiency with grumose degeneration in the dentate nucleus of the cerebellum. The patient had intractable neonatal convulsions and hyperammonemia from the 3rd day after birth. Diagnosis of OTC deficiency was made based on null activity of the enzyme and four-base deletions in exon 9 of the OTC gene. Death was due to sepsis as well as disseminated intravascular coagulation at I year and 2 months of age. Neuropathology showed multiple cystic changes and ulegyria in the bilateral frontal and parietal lobes. Multiple cysts were associated with the region, which was infiltrated with macrophages surrounded by astroglia showing palisading pattern, Ferrugination was marked in the thalamus and severe neuronal loss with astrogliotic change in the CA1-2 area of the hippocampus. Grumose degeneration was noted in the dentate nucleus of the cerebellum. This is the first report of grumose degeneration in OTC deficiency. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:91 / 94
页数:4
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