由ATAD3A新型变异引起的哈雷尔-尤恩综合征:一个病例报告
Shuning Zhang1,2, Luyao Lin1, Yuelin Li1
1Department of NICU, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian, 350001, PR China.
Heliyon
|January 4, 2024
概括
这项研究详细介绍了一种新的ATAD3A基因突变,导致新生儿出现哈雷尔-尤恩综合征. 早期识别这些ATAD3A变异对于及时诊断和干预至关重要.
科学领域:
- 遗传学 遗传学 是一个
- 临床医学 临床医学
- 罕见疾病 罕见疾病
背景情况:
- 哈雷尔-尤恩综合征是一种罕见的遗传性疾病.
- ATAD3A基因变异与各种表型有关.
- 新生儿出现的哈雷尔-尤恩综合征的特征并不清楚.
研究的目的:
- 描述一个患有哈雷尔-尤恩综合征的新生儿的临床特征.
- 为了确定观察到的表型的遗传基础.
- 扩大对ATAD3A相关疾病的理解.
主要方法:
- 一个患有哈雷尔-尤恩综合征的新生儿的案例研究.
- 对试验物进行临床和放射学评估.
- 整体外组测序和PCR-桑格测序用于基因分析.
主要成果:
- 新生儿出现了严重的新生儿症状,包括发作,喉,低血压,食困难和角膜不透明.
- 在ATAD3A基因中发现了一种新型异构基单基替代 (c.1517A > C; p.Q506P).
- 患者患有呼吸衰竭,随后死亡.
结论:
- 这项研究报告了一种新的ATAD3A突变,扩大了已知的ATAD3A相关疾病的范围.
- 新生儿临床特征的全面描述有助于识别ATAD3A相关的哈雷尔-尤恩综合征 (HAYOS).
- 早期识别ATAD3A变异对于管理这种严重疾病至关重要.
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