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腺苷酸琥珀酸裂解酶缺乏症:首例确诊的波兰患者。

Adenylosuccinate lyase deficiency: the first identified polish patient.

作者信息

Jurkiewicz Elzbieta, Mierzewska Hanna, Kuśmierska Katarzyna

机构信息

The Children's Memorial Health Institute, MR Unit, Al. Dzieci Polskich 20, 04-730 Warsaw, Poland.

出版信息

Brain Dev. 2007 Oct;29(9):600-2. doi: 10.1016/j.braindev.2007.03.005. Epub 2007 May 7.

Abstract

Adenylosuccinate lyase (ADSL) deficiency is a rare disease of de novo purine synthesis. The main symptoms are psychomotor retardation, epilepsy, autistic features, occasionally associated with muscular hypotonia. Diagnosis is made by detection of abnormal purine metabolites (succinyladenosine - S-Ado and succinylaminoimidazole carboxamide riboside - SAICAr) in body fluids. The severity of the clinical features correlates with low S-Ado/SAICAr ratio. We report clinical, biochemical and brain MRI findings of a female infant with severe early epilepsy and hypotonia, who died at the age of 10 weeks.

摘要

腺苷酸琥珀酸裂解酶(ADSL)缺乏症是一种罕见的从头嘌呤合成疾病。主要症状为精神运动发育迟缓、癫痫、自闭症特征,偶尔伴有肌张力减退。通过检测体液中异常的嘌呤代谢产物(琥珀酰腺苷 - S - Ado和琥珀酰氨基咪唑甲酰胺核苷 - SAICAr)进行诊断。临床特征的严重程度与低S - Ado/SAICAr比值相关。我们报告了一名患有严重早期癫痫和肌张力减退的女婴的临床、生化和脑部MRI检查结果,该女婴在10周龄时死亡。

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