Hoebeke C, Cano A, De Lonlay P, Chabrol B
Inborn Error of Metabolism Reference Centre, La Timone Teaching Hospital, 264, rue Saint-Pierre, 13385 Marseille, France.
Inborn Error of Metabolism Reference Centre, La Timone Teaching Hospital, 264, rue Saint-Pierre, 13385 Marseille, France.
Arch Pediatr. 2021 Jan;28(1):80-86. doi: 10.1016/j.arcped.2020.11.004. Epub 2020 Dec 17.
The clinical picture associated with a Transport and Golgi Organization 2 (TANGO2) gene bi-allelic mutation is represented by encephalopathy and rhabdomyolysis marked by cardiac rhythm disorders and neurological regression. The presentation of encephalopathy is diverse and can range from isolated language delay and cognitive impairment in a child to multiple disabilities and spastic quadriparesis. Hypothyroidism has also been frequently reported. This article presents the clinical phenotype of seven children with a TANGO2 bi-allelic mutation. The mutation was found by sequencing a panel of genes associated with rhabdomyolysis. While the clinical picture represents generalized cases, there is phenotypic variability in, for example, the degree of disability for each patient. A TANGO2 gene mutation, nevertheless, represents a serious illness with a limited life expectancy due to an unpredictable risk of cardiac rhythm disorder and death, particularly during rhabdomyolysis. Although the natural history of the disease presents an evolution of rhabdomyolysis triggered by infections or effort, an early diagnosis is difficult due in part to the fact that there is a lack of specific biochemical marker or identifying symptoms in the early presentation of the disease. Clinicians must therefore consider the TANGO2 gene when confronted with rhabdomyolysis in a patient suffering from an early developmental disorder. In the meantime, management of the disease remains purely symptomatic.
与转运和高尔基体组织2(TANGO2)基因双等位基因突变相关的临床症状表现为脑病和横纹肌溶解,其特征为心律失常和神经功能衰退。脑病的表现多样,从儿童单纯的语言发育迟缓及认知障碍到多重残疾和痉挛性四肢瘫。甲状腺功能减退也屡有报道。本文介绍了7例携带TANGO2双等位基因突变患儿的临床表型。该突变是通过对一组与横纹肌溶解相关的基因进行测序发现的。虽然临床症状代表了普遍情况,但每个患者的残疾程度等存在表型差异。然而,由于存在心律失常和死亡的不可预测风险,尤其是在横纹肌溶解期间,TANGO2基因突变代表一种严重疾病,预期寿命有限。尽管该疾病的自然病程表现为由感染或劳累引发的横纹肌溶解的进展,但早期诊断困难,部分原因是在疾病早期缺乏特异性生化标志物或识别症状。因此,当面对患有早期发育障碍且出现横纹肌溶解的患者时,临床医生必须考虑TANGO2基因。与此同时,该疾病的治疗仍仅为对症治疗。