TANGO-2:一种罕见的遗传性疾病,临床上表现为脑病、横纹肌溶解和2例儿童心律失常。

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Khairunnisa Mukhtiar, Shahnaz Ibrahim, Quart-Ul-Ain Khalid
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引用次数: 0

摘要

转运体和高尔基组织2 (TANGO-2)的双等位基因致病性或可能致病性变异与一系列临床特征相关,包括脑病、横纹肌溶解、心律失常和神经功能减退。我们报告了2例无血缘关系的双等位基因TANGO-2致病性变异患儿。这些变异是通过与遗传性横纹肌溶解相关的下一代测序(NGS)基因小组确定的。两个孩子都有发育迟缓的历史,尤其是在运动方面。他们还经历了急性疾病的短暂性虚弱。其中一个孩子的兄弟姐妹也有类似的症状,很早就去世了。在他们的疾病期间,两个孩子都出现了极度嗜睡,CPK水平非常高,乳酸酸中毒,转氨酶上升趋势,反复低血糖。两例患者均出现室性心动过速,超声心动图显示心肌病。尽管进行了强化的症状治疗,但两例患者均死于致命性室性心律失常引起的心力衰竭。基因检测显示存在双等位基因致病变异TANGO-2。这种罕见的遗传性疾病在任何出现间歇性复发性虚弱、横纹肌溶解、腹痛和心律失常的患者中都应被怀疑,因为其临床表现多样。然而,早期诊断具有挑战性,因为这种疾病没有特定的生化标志物。有强有力的证据表明,补充维生素B可以显著减少这些儿童的代谢危机。虽然这不是一种靶向治疗,但对于这些患者来说,它可能是一种挽救生命的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TANGO-2: A Rare Genetic Condition With Severe Clinical Presentation of Encephalopathy, Rhabdomyolysis, and Cardiac Rhythm Disorders in 2 Children.

Biallelic pathogenic or likely pathogenic variants in Transport and Golgi Organization 2 (TANGO-2) are associated with a spectrum of clinical features including encephalopathy, rhabdomyolysis, cardiac rhythm disorders, and neurologic regression. We are reporting on 2 unrelated children with biallelic TANGO-2 pathogenic variants. These variants were identified through a Next Generation Sequencing (NGS) panel of genes associated with hereditary rhabdomyolysis. Both children had a history of developmental delay, especially in their motor milestones. They also experienced episodic transient weakness with acute illness. One of the children's siblings had similar complaints and died at an early age. During their illness, both children developed extreme lethargy with very high CPK levels, lactic acidosis, rising trends of transaminases, and recurrent hypoglycemia. Both patients developed ventricular tachyarrhythmias, and the echocardiogram showed cardiomyopathy. Despite intensive symptomatic management, both patients died of cardiac failure because of fatal ventricular arrhythmia. Genetic testing revealed the presence of biallelic pathogenic variants TANGO-2. This rare genetic condition should be suspected in any patient with episodic recurrent weakness, rhabdomyolysis, abdominal pain, and cardiac arrhythmias, because of its diverse clinical presentation. However, early diagnosis is challenging because there are no specific biochemical markers for the disease. There is strong evidence that vitamin B supplementation can significantly reduce the number of metabolic crises in these children. Although this is not a targeted therapy, it can be a potentially life-saving treatment for these patients.

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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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