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缩短的胎儿长骨:在SHOX相关的骨发育不良症中,这是一个显著的子宫内表型特征
Rong Hu1,2, Weiwei Huang1,2, Congmian Ren1,2
1Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, China.
Prenatal diagnosis
|August 1, 2023
概括
矮身高的含有SHOX基因的微删除会导致胎儿长骨缩短. 通过超声波和SNP-array的早期产前诊断有助于管理SHOX相关的骨发育不良.
科学领域:
- 遗传学 遗传学 是一个
- 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:
- 矮身高的含有家庭盒子 (SHOX) 基因突变与骨失调有关.
- 了解子宫内表型谱对于遗传咨询至关重要.
研究的目的:
- 为了划分SHOX基因相关的骨发育不良的子宫内表型谱.
- 为风险怀孕的遗传咨询提供指导.
主要方法:
- 通过单核酸多态 (SNP) 阵列识别的SHOX微删除胎儿的分析.
- 详细检查子宫内表现型和结果.
主要成果:
- 有SHOX微删除 (0.1341.35 Mb) 的9个胎儿显示长骨缩短 (-2.0至-5.3 SD).
- 特定的股骨/脚和股骨/腹周比表明非致命的骨发育不良.
- 其他发现包括子宫内生长限制和鼻骨缺血;马德龙形缺席.
结论:
- SHOX 哈普隆缺陷可以呈现为缩短的胎儿长骨.
- 结合临床病史,产前超声波和SNP-array,可以早期诊断和治疗SHOX相关的骨发育不良.
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