关节,功能障碍,胆固醇症候群与两个兄弟姐妹的新奇突变
Rahiya Rehman1,2,3,4, Leslia Gonzalez1,3,4, Kelsey Kolbe3
1Department of Pediatrics Warren Alpert Medical School/Brown University Providence Rhode Island USA.
Clinical case reports
|May 3, 2024
概括
这一案例系列突出显示了与关节形症,功能障碍和胆固醇症 (ARC) 综合征相关的新变异. 早期基因检测对于婴儿发育不良,脏问题和病至关重要,即使是轻度胆固醇,以改善结果.
科学领域:
- 遗传学和罕见疾病.
- 儿科病学 儿科病学
- 肝病学 肝病学是一种肝病学.
背景情况:
- 关节,功能障碍和胆固醇症候群 (ARC) 是一种罕见的遗传性疾病.
- 遗传变异与ARC综合征的发病有关.
- 临床表现可能会有所不同,这会给诊断带来挑战.
研究的目的:
- 描述与ARC综合征相关的新型变异.
- 强调早期诊断和在疑似病例中进行遗传检测的重要性.
- 突出那些需要对ARC综合征进行调查的临床特征.
主要方法:
- 报告临床和遗传发现的案例系列.
- 对具有暗示ARC综合征的特征的患者进行审查.
- 基因分析以确定致病变体.
主要成果:
- 识别有助于ARC相关突变谱的新变异.
- 证明管功能障碍和恶心病可以很突出,即使是轻度胆固醇.
- 特定临床表现与已识别的遗传变异的相关性.
结论:
- 需要提高对ARC相关变异的认识.
- 应该考虑在婴儿中进行基因检测,这些婴儿的发育不良,管功能障碍和恶心病.
- 及时诊断和干预可能会改善患者的生活质量.
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