现型扩展:胎儿与科尔-木匠类型2呈现与新生儿致命骨失生症
Natalie Burrill1, Christina Paidas Teefey2,3, Renee Wright2
1The Children's Hospital of Philadelphia, Department of Pediatrics, Individualized Medical Genetics Center, Philadelphia, Pennsylvania, USA.
American journal of medical genetics. Part A
|January 9, 2025
概括
这项研究详细介绍了一种罕见的,严重的Cole-Carpenter综合征2型 (CLCRP2) 产前表现,导致新生儿早期死亡. 这些发现突出了CLCRP2.2以前未报告的限制生命的表型.
科学领域:
- 医学遗传学 医学遗传学
- 产前诊断 在产前诊断
- 骨发育不良症 骨发育不良症
背景情况:
- 科尔-卡宾特综合征2型 (CLCRP2) 通常呈现出一个有利的预后.
- 严重的产前骨发育不良可能是具有挑战性的诊断和管理.
研究的目的:
- 报告一个独特的,限制生命的CLCRP2.2产前病例.
- 描述这种严重表现的遗传和表型特征.
主要方法:
- 胎儿超声波用于骨异常的评估.
- 通过皮取样本进行外体序列测序,用于基因诊断.
- 图像和遗传发现的临床相关性.
主要成果:
- 胎儿超声检查显示严重的骨发育不良,生长受限,以及模仿致命骨质变异不完美的特征.
- 外体测序发现了可能的致病性SEC24D变体和VUS,与CLCRP2.2一致.
- 胎儿由于呼吸道受损而经历了新生儿早期死亡.
结论:
- 这种病例代表了首次报告的CLCRP2.2的限制生命的产前表型.
- 严重的表现是致命的骨疾病的副本,扩大了已知的CLCRP2.2谱.
- 基因分析对于诊断非典型的骨发育不良的表现至关重要.
关键词:
美国证券交易委员会SEC24D科尔-卡宾特综合征2型外基因组测序是指外基因组的测序.骨质发生不完美 (osteogenesis imperfecta) 是一个不完美的疾病.围产期限制生命的产后药物产前诊断 产前诊断 产前诊断更多相关视频
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