联合氧化酸化缺乏症的表型划分-12:两名患者的临床特征
Meral Bahar Ister1, Muge Cinar1, Serdar Ceylaner2
1Faculty of Medicine, Pediatric Metabolism, Kocaeli University, Kocaeli, Turkey.
联合氧化酸化缺陷-12 (COXPD12) 是一种罕见的疾病. 这项研究确定了两名患者独特的面部特征,有助于COXPD12诊断.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
- 生物化学 生物化学
背景情况:
- 组合氧化酸化缺陷-12 (COXPD12) 是一种罕见的自体相衰退性疾病.
- 神经症状和乳酸性酸是COXPD12的常见表现.
研究的目的:
- 描述两名COXPD患者的新型,一致的异形面部特征12.
- 突出COXPD12中面部表型的诊断实用性.
主要方法:
- 两名COXPD患者的临床病例表现12.
- 脸部异形特征的详细描述.
- 头骨MRI分析.
- 对EARS2基因变异的分子遗传分析.
主要成果:
- 在这两位患者中都观察到相同的,以前未被描述的异形面部特征.
- 两位患者都出现了低血压和乳酸性酸症.
- 核磁共振扫描显示白质扩散受限和低髓化.
- 基因分析发现了EARS2变异,其中包括一个患者的新型变异.
结论:
- 典型的面部特征可以作为COXPD的关键诊断线索12.
- 早期识别面部表型有助于诊断这种罕见的疾病.
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