Angie El-Said, Jorge Luis Morales, Gian Rossi, Neha Longani
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One individual was treated with l-arginine, ubiquinol, and levocarnitine. The other individual recovered without any intervention.</p><p><strong>Discussion: </strong>ZTTK syndrome is a rare condition caused by pathogenic variants in <i>SON</i>. This syndrome is characterized by global developmental delay, short stature, facial dysmorphisms, seizures, hypotonia, and brain abnormalities. A metabolic stroke has not been reported as a common manifestation. <i>SON</i> has been reported to play a role in mitochondrial function. This can explain why metabolic stroke can be seen in individuals with ZTTK syndrome. 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引用次数: 0
摘要
目的:本研究报告了2例无亲和关系的zhuo - tokita - takenouchi - kim (ZTTK)综合征患者表现为代谢性卒中,而代谢性卒中通常未被报道为该综合征的临床表现。方法:两名女性儿童在代谢性卒中就诊后被诊断为ZTTK综合征,因为他们的临床特征和先前的基因检测显示SON的致病变异。结果:两例患者均表现为急性左偏瘫。他们接受了检查,并通过脑MRI确定了相应的代谢性中风。两个人都恢复了良好的功能结果。一名患者接受l-精氨酸、泛醇和左卡尼汀治疗。另一个人在没有任何干预的情况下康复了。讨论:ZTTK综合征是一种罕见的由SON致病变异引起的疾病。该综合征的特点是全面发育迟缓、身材矮小、面部畸形、癫痫发作、张力低下和大脑异常。代谢性中风并没有作为一种常见的表现被报道。据报道,SON在线粒体功能中起作用。这可以解释为什么代谢性中风可以在患有ZTTK综合征的个体中看到。重要的是要认识到代谢性卒中可能是ZTTK综合征的临床表现,因为它具有临床和治疗意义。
Metabolic Stroke as a Clinical Manifestation of Zhu-Tokita-Takenouchi-Kim Syndrome: A Case Series.
Objective: This study reports 2 unrelated individuals with Zhu-Tokita-Takenouchi-Kim (ZTTK) syndrome who presented with a metabolic stroke, which has not been commonly reported as a clinical manifestation of this syndrome.
Methods: Two female children were identified after presenting to our institution with a metabolic stroke and carried a diagnosis of ZTTK syndrome because of their clinical characteristics and previous genetic testing demonstrating pathogenic variants in SON.
Results: Both individuals presented with acute-onset left hemiplegia. They underwent workup, and corresponding metabolic stroke was identified on brain MRI. Both individuals recovered with good functional outcome. One individual was treated with l-arginine, ubiquinol, and levocarnitine. The other individual recovered without any intervention.
Discussion: ZTTK syndrome is a rare condition caused by pathogenic variants in SON. This syndrome is characterized by global developmental delay, short stature, facial dysmorphisms, seizures, hypotonia, and brain abnormalities. A metabolic stroke has not been reported as a common manifestation. SON has been reported to play a role in mitochondrial function. This can explain why metabolic stroke can be seen in individuals with ZTTK syndrome. It is important to recognize that metabolic stroke can be a clinical manifestation of ZTTK syndrome because it carries clinical and therapeutic implications.
期刊介绍:
Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.