在产前诊断出Pfeiffer综合征与多囊的罕见病例
Poornima Sharma1, Shreya Singh Kushwaha1, Suchandana Dasgupta1
1Fetal Medicine Division, Department of Obstetrics and Gynaecology, VMMC and Safdarjung Hospital, New Delhi, India.
Journal of obstetrics and gynaecology of India
|May 20, 2025
概括
费弗氏综合征是一种罕见的遗传疾病,导致头骨骨和明显的面部特征的过早融合. 纤维细胞生长因子受体 (FGFR1或FGFR2) 的突变是主要原因,导致不同的临床表现.
科学领域:
- 医学遗传学 医学遗传学
- 发展生物学 发展生物学
- 儿科医学 儿科医学
背景情况:
- 费弗氏综合征是一种罕见的关突症,影响头骨发育.
- 它的特征是冠状结合症,中脸过度成形和四肢异常.
- 由纤维细胞生长因子受体 (FGFR1/FGFR2) 的突变引起.
研究的目的:
- 要总结Pfeiffer综合征的关键特征和遗传基础.
- 突出该疾病的临床和遗传异质性.
- 审查产前诊断的诊断时间和罕见性.
主要方法:
- 关于Pfeiffer综合征病例的文献综述.
- 对纤维细胞生长因子受体中的遗传突变进行分析.
- 临床表型和诊断标准的评估.
主要成果:
- 费弗氏综合征表现为双边冠状骨同位症,中间面部低成形,鼻子,以及指/脚异常.
- 自体主导遗传是典型的,与FGFR1或FGFR2基因突变有关.
- 存在显著的临床和遗传变异性,大多数病例都是新生儿诊断的.
结论:
- 费弗综合征是一种遗传异质性疾病,具有明显的面和四肢异常.
- FGFR1/FGFR2突变是潜在的原因,以自体主导模式遗传.
- 产前诊断不常见,大多数病例是在产后发现的.
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