在一个患有自闭症谱系障碍和大脑症的孩子中,一种新型PTEN变异:一个案例报告
Margarida Moreno Fernandes1, Mariana Rodrigues Neto1, Mariana Sá Pinto1
1Pediatrics, Unidade Local de Saúde Gaia/Espinho, Vila Nova de Gaia, PRT.
Cureus
|February 6, 2026
概括
PTEN hamartoma瘤综合征 (PHTS) 是一种罕见的遗传疾病. 在患有自闭症和巨头症的儿童中,早期识别对于及时诊断和监测至关重要.
科学领域:
- 遗传学 遗传学 是一个
- 儿科 儿科 儿科
- 神经学 神经学
背景情况:
- PTEN hamartoma瘤综合征 (PHTS) 是一种罕见的遗传疾病,与神经发育障碍,巨头症和癌症倾向有关.
- 患有PHTS的儿童经常表现出一系列症状,包括发育迟缓和巨头症.
研究的目的:
- 报告一个患有自闭症谱系障碍 (ASD) 和大脑的年轻女孩的PHTS病例.
- 突出在儿科患者中怀疑PHTS的关键临床指标.
- 强调早期遗传诊断和对PTEN相关疾病的监测的重要性.
主要方法:
- 一个四岁女孩的案例报告.
- 临床评估包括神经成像 (MRI) 和遗传检测.
- 在PTEN基因中发现了一种新型的框架转移变异.
主要成果:
- 这名患者出现了先天性甲状腺功能低下症,渐进性大脑症,全身发育迟缓,后来被诊断为ASD.
- 大脑MRI显示大脑大脑与扩大的外轴空间和加厚的体.
- 基因分析揭示了PTEN基因中的一种新型的移变异.
结论:
- 这一案例强调了在患有自闭症和巨头症的儿童中考虑PHTS的重要性,即使没有明显的瘤症状.
- 早期识别PTEN相关疾病有助于快速基因诊断和实施适当的监测协议.
- 早期识别PHTS可以导致更好的管理和改善受影响儿童的结果.
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