病例报告:多系统光滑肌肉功能障碍综合征:婴儿间歇性肺病的罕见遗传原因
Qianying Li1, Lidan Cui1, Jun Su1
1Pediatric Intensive Care Unit, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, China.
Frontiers in pharmacology
|January 27, 2025
概括
多系统光滑肌肉功能障碍综合征 (MSMDS) 可以呈现为婴儿间歇性肺病 (ILD). 早期诊断和考虑ACTA2基因变异对于这种罕见的疾病至关重要.
科学领域:
- 遗传学和罕见疾病
- 儿科肺病学 儿科肺病学
- 心血管医学 心血管医学
背景情况:
- 多系统平滑肌肉功能障碍综合征 (MSMDS) 是一种自体主导遗传疾病.
- ACTA2基因的突变是MSMDS的已知原因,导致多器官功能障碍.
- 间歇性肺病 (ILD) 是MSMDS的不常见但严重的表现.
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