Sarangi Pradosh Kumar, Sahoo Lulup Kumar, Mallick Ashok Kumar, Dash Prafulla Kumar
Department of Radiodiagnosis, S.C.B. Medical College, Cuttack, Odisha, India.
Department of Neurology, S.C.B. Medical College, Cuttack, Odisha, India.
J Pediatr Neurosci. 2017 Jan-Mar;12(1):85-86. doi: 10.4103/jpn.JPN_165_16.
Glutaric aciduria type I (GA I) is an autosomal recessive inborn error of metabolism caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. This disorder is characterized by progressive dystonia, choreoathetosis, and dyskinesia. It is often misdiagnosed as athetoid cerebral palsy. Laboratory evaluation usually demonstrates increased urinary excretion of gluataric acid and 3-hydroxyglutaric acid. We report a case of a 7-year-old boy presenting with choreoathetosis and dystonia, mimicking as choreoathetoid cerebral palsy. The presence of characteristic neuroimaging and biochemical studies led to the diagnosis of GA I.
I型戊二酸血症(GA I)是一种常染色体隐性遗传的先天性代谢紊乱疾病,由戊二酰辅酶A脱氢酶缺乏引起。这种病症的特征是进行性肌张力障碍、舞蹈手足徐动症和运动障碍。它常被误诊为手足徐动型脑瘫。实验室检查通常显示尿中戊二酸和3-羟基戊二酸排泄增加。我们报告一例7岁男孩,表现为舞蹈手足徐动症和肌张力障碍,类似舞蹈手足徐动型脑瘫。特征性的神经影像学和生化研究结果确诊为GA I。