哺乳困难的婴儿的遗传表现和表型谱
Mingyu Han1,2, Wei Shi2,3, Xiangxiang Chen1,2
1Department of Neonatology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Molecular genetics & genomic medicine
|August 28, 2024
概括
婴儿的食困难可能是罕见遗传疾病的信号. 整体外因子测序 (WES) 有助于识别遗传原因,改善了这些复杂病例的诊断.
科学领域:
- 儿科遗传学 儿科遗传学
- 新生儿科学 新生儿科学
- 罕见疾病 罕见疾病
背景情况:
- 在患有罕见遗传疾病的婴儿中,食困难很常见.
- 这些挑战往往是多系统条件的一部分.
研究的目的:
- 鉴定养困难的婴儿遗传发现的特征.
- 探索与这些遗传条件相关的表型谱.
主要方法:
- 分析了6个月以下有食困难的婴儿病例系列.
- 在所有参与者身上进行了全外体测序 (WES).
- 临床表型和遗传结果是相关的.
主要成果:
- 28名婴儿中有22名 (78.3%) 患有由WES.发现的与疾病相关的遗传变异.
- 15名婴儿 (53.6%) 获得了确定的遗传诊断.
- 异常的肌肉度和神经问题普遍存在;96.2%的人有头骨MRI异常.
结论:
- 食困难可能是罕见遗传疾病的关键指标.
- WES显著提高了婴儿出现食问题的诊断准确度.
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