Sen Kuntal, Castillo Pinto Carlos, Gropman Andrea L
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.
J Pediatr Genet. 2021 Mar;10(1):77-80. doi: 10.1055/s-0040-1709670. Epub 2020 Apr 23.
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.
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。