结节性硬化
TSC1
TSC2
胎儿
医学
儿科
室管膜下巨细胞星形细胞瘤
遗传咨询
产前诊断
室管膜下区
遗传性疾病
怀孕
病理
生物
遗传学
疾病
胶质母细胞瘤
星形细胞瘤
细胞凋亡
癌症研究
PI3K/AKT/mTOR通路
作者
Anna S. Bolshakova,D.N. Maslennikov,Jekaterina Shubina,Andrey A. Bystritskiy,Ekaterina Tolmacheva,I. S. Mukosey,Т. О. Кочеткова,Grigory S. Vasiliev,Ekaterina E. Atapina,Igor Sadelov,Nadezhda Zaretskaya,I. Yu. Barkov,D.N. Degtyarev,D. Yu. Trofimov
标识
DOI:10.1136/jcp-2023-208935
摘要
We describe the clinical and genetic characteristics of fetuses and infants diagnosed with tuberous sclerosis complex (TSC) in our centre, prenatally or neonatally, for a better understanding of the benefits of early screening.
科研通智能强力驱动
Strongly Powered by AbleSci AI