Suppr超能文献

质子磁共振波谱的扩展作用:鸟氨酸转氨甲酰酶部分缺乏症的及时诊断与治疗启动

Expanding Role of Proton Magnetic Resonance Spectroscopy: Timely Diagnosis and Treatment Initiation in Partial Ornithine Transcarbamylase Deficiency.

作者信息

Sen Kuntal, Castillo Pinto Carlos, Gropman Andrea L

机构信息

Division of Neurogenetics and Developmental Pediatrics, Center for Neuroscience and Behavioral Medicine, Children's National Hospital, Washington, District of Columbia, United States.

Center for Neuroscience and Behavioral Medicine, Children's National Hospital, Washington, District of Columbia, United States.

出版信息

J Pediatr Genet. 2021 Mar;10(1):77-80. doi: 10.1055/s-0040-1709670. Epub 2020 Apr 23.

Abstract

We report the case of a 3-year-old male patient who presented with a 3-day history of altered mental status, emesis, and abdominal pain in the setting of a viral illness. A rapid screening revealed a high ammonia level and after reviewing his proton magnetic resonance spectroscopy (1H MRS) which showed the classic triad of high glutamate, low choline, and myoinositol, a diagnosis of ornithine transcarbamylase deficiency (OTCD) was made within 6 hours of presentation. Therapy with sodium phenylbutyrate and sodium benzoate was initiated and patient was discharged after 3 days with no neurologic disability. Biochemical and molecular testing eventually confirmed the diagnosis. 1H MRS is a practical and fast neuroimaging modality that can aid in diagnosis of OTCD and enables faster initiation of treatment in acute settings.

摘要

我们报告了一例3岁男性患者,在病毒感染性疾病背景下,出现精神状态改变、呕吐和腹痛3天。快速筛查显示血氨水平升高,在查看其质子磁共振波谱(1H MRS)显示谷氨酸水平高、胆碱和肌醇水平低的典型三联征后,在就诊后6小时内诊断为鸟氨酸转氨甲酰酶缺乏症(OTCD)。开始使用苯丁酸钠和苯甲酸钠治疗,3天后患者出院,无神经功能障碍。生化和分子检测最终确诊。1H MRS是一种实用且快速的神经成像方式,可有助于OTCD的诊断,并能在急性情况下更快地开始治疗。

相似文献

3
Antepartum ornithine transcarbamylase deficiency.
Case Rep Gastroenterol. 2014 Nov 5;8(3):337-45. doi: 10.1159/000369131. eCollection 2014 Sep-Dec.
4
Late-Onset Ornithine Transcarbamylase Deficiency and Variable Phenotypes in Vietnamese Females With Mutations.
Front Pediatr. 2020 Jul 23;8:321. doi: 10.3389/fped.2020.00321. eCollection 2020.
5
Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.
Radiology. 2009 Sep;252(3):833-41. doi: 10.1148/radiol.2523081878. Epub 2009 Jun 30.
9
Ornithine Transcarbamylase Deficiency Presenting as Acute Encephalopathy After Strabismus Surgery.
Cureus. 2022 Jul 8;14(7):e26667. doi: 10.7759/cureus.26667. eCollection 2022 Jul.
10
1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.
Mol Genet Metab. 2008 Sep-Oct;95(1-2):21-30. doi: 10.1016/j.ymgme.2008.06.003. Epub 2008 Jul 26.

引用本文的文献

1
Dysregulation of Astrocytic Glutamine Transport in Acute Hyperammonemic Brain Edema.
Front Neurosci. 2022 Jun 6;16:874750. doi: 10.3389/fnins.2022.874750. eCollection 2022.
2
Neuromonitoring in Rare Disorders of Metabolism.
Yale J Biol Med. 2021 Dec 29;94(4):645-655. eCollection 2021 Dec.
3
Fifteen years of urea cycle disorders brain research: Looking back, looking forward.
Anal Biochem. 2022 Jan 1;636:114343. doi: 10.1016/j.ab.2021.114343. Epub 2021 Oct 9.

本文引用的文献

2
Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update.
J Genet Genomics. 2015 May 20;42(5):181-94. doi: 10.1016/j.jgg.2015.04.003. Epub 2015 May 19.
3
Inborn errors of metabolism.
Clin Perinatol. 2015 Jun;42(2):413-39, x. doi: 10.1016/j.clp.2015.02.010. Epub 2015 Apr 8.
5
The incidence of urea cycle disorders.
Mol Genet Metab. 2013 Sep-Oct;110(1-2):179-80. doi: 10.1016/j.ymgme.2013.07.008. Epub 2013 Jul 18.
6
Neuroimaging in mitochondrial disorders.
Neurotherapeutics. 2013 Apr;10(2):273-85. doi: 10.1007/s13311-012-0161-6.
7
Brain magnetic resonance spectroscopy in episodic hepatic encephalopathy.
J Cereb Blood Flow Metab. 2013 Feb;33(2):272-7. doi: 10.1038/jcbfm.2012.173. Epub 2012 Nov 21.
8
Brain imaging in urea cycle disorders.
Mol Genet Metab. 2010;100 Suppl 1(Suppl 1):S20-30. doi: 10.1016/j.ymgme.2010.01.017. Epub 2010 Feb 13.
9
1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.
Mol Genet Metab. 2008 Sep-Oct;95(1-2):21-30. doi: 10.1016/j.ymgme.2008.06.003. Epub 2008 Jul 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验