由新基因突变诊断出婴儿阿尔斯特罗姆综合征:一个病例报告
Yujiao Ye1, Xianmin Wang1, Guixia Li1
1Department of Pediatrics, Sichuan Provincial Maternity and Child Health Care Hospital, Women and Children's Hospital Affiliated to Chengdu Medical College, Chengdu, Sichuan Province, China.
The Journal of international medical research
|July 13, 2023
概括
阿尔斯特罗姆综合征是一种罕见的遗传疾病,在婴儿身上使用全外组测序来诊断. 这一案例凸显了基因测试对于早期阿尔斯特罗姆综合征识别的重要性.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 罕见疾病 罕见疾病
背景情况:
- 阿尔斯特罗姆综合征是一种罕见的自体相衰退性遗传疾病.
- 它是由ALMS1基因的突变引起的.
- 早期诊断对于管理这种情况至关重要.
研究的目的:
- 提交诊断为阿尔斯特罗姆综合征的婴儿的临床数据.
- 为了确定在这种情况下负责这种情况的特定ALMS1基因突变.
- 强调整体外组测序在诊断阿尔斯特罗姆综合征中的作用.
主要方法:
- 从一个2个月大的男婴收集临床数据.
- 诊断严重的肺炎,急性充血性心力衰竭和心肌炎.
- 整体外基因组测序以识别遗传突变.
主要成果:
- 婴儿出现了严重的呼吸道和心脏症状.
- 整个外体序列测序揭示了ALMS1基因中的复合异构基因突变:c.2179dup (p. Y727Lfs*12) 和c.11140C>T (p. Q3714*).
- 根据ACMG指导方针,这两种发现的突变都被归类为致病性.
结论:
- 在这个婴儿身上发现了一种新的ALMS1突变.
- 基因检测,特别是全外因组测序,对于早期和准确诊断阿尔斯特罗姆综合征至关重要.
- 这一案例强调了阿尔斯特罗姆综合征在婴儿中的遗传异质性和临床表现.
关键词:
这是ALMS1基因.阿尔斯特罗姆综合征是什么意思心肌病性心脏病 - 心肌病性心脏病案例报告案例报告超声心电图 (Echocardiography) 是一种心声回声仪.基因检测 基因检测是指基因检测.更多相关视频
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