Prenatal genetic considerations in congenital ventriculomegaly and hydrocephalus

被引：0
|
作者：
Adolfo Etchegaray
Sofia Juarez-Peñalva
Florencia Petracchi
Laura Igarzabal
机构：
[1] Hospital Universitario Austral,Unidad de Medicina Fetal
[2] CEMIC,Servicio de Genética
来源：
Child's Nervous System | 2020年 / 36卷
关键词：
Fetal ventriculomegaly; Congenital hydrocephalus; Prenatal diagnosis; Prenatal genetic testing;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：1645 / 1660
页数：15
相关论文
共 50 条
  • [41] Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects
    Schmid, Maximilian
    Stary, Susanne
    Blaicher, Wibke
    Gollinger, Michaela
    Husslein, Peter
    Streubel, Berthold
    PRENATAL DIAGNOSIS, 2012, 32 (04) : 376 - 382
  • [42] Prenatal Genetic Testing Options
    Jelin, Angie C.
    Sagaser, Katelynn G.
    Wilkins-Haug, Louise
    PEDIATRIC CLINICS OF NORTH AMERICA, 2019, 66 (02) : 281 - +
  • [43] External hydrocephalus as a prenatal feature of noonan syndrome
    Mastromoro, Gioia
    De Luca, Alessandro
    Marchionni, Enrica
    Spagnuolo, Antonella
    Ventriglia, Flavia
    Manganaro, Lucia
    Pizzuti, Antonio
    ANNALS OF HUMAN GENETICS, 2021, 85 (06) : 249 - 252
  • [44] Evaluation of functional outcomes in congenital hydrocephalus
    Venkataramana, N. K.
    Mukundan, C. R.
    JOURNAL OF PEDIATRIC NEUROSCIENCES, 2011, 6 (01) : 4 - 12
  • [45] Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies
    Cai, Meiying
    Huang, Hailong
    Xu, Liangpu
    Lin, Na
    FRONTIERS IN GENETICS, 2021, 12
  • [46] Fetal brain damage in congenital hydrocephalus
    Maria Florencia Varela
    Marcos M. Miyabe
    Marc Oria
    Child's Nervous System, 2020, 36 : 1661 - 1668
  • [47] Fetal brain damage in congenital hydrocephalus
    Varela, Maria Florencia
    Miyabe, Marcos M.
    Oria, Marc
    CHILDS NERVOUS SYSTEM, 2020, 36 (08) : 1661 - 1668
  • [48] Prenatal findings and associated survival rates in fetal ventriculomegaly: A prospective observational study
    Ryan, Gillian A.
    Start, Alexander O.
    Cathcart, Barbara
    Hughes, Heather
    Denona, Branko
    Higgins, Shane
    Corcoran, Siobhan
    Walsh, Jennifer
    Carroll, Stephen
    Mahony, Rhona
    Crimmins, Darach
    Caird, John
    Robinson, Ian
    Colleran, Gabrielle
    McParland, Peter
    McAuliffe, Fionnuala M.
    INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2022, 159 (03) : 891 - 897
  • [49] The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study
    Mone, Fionnuala
    Stott, Bethany K.
    Hamilton, Susan
    Seale, Anna N.
    Quinlan-Jones, Elizabeth
    Allen, Stephanie
    Hurles, Matthew E.
    McMullan, Dominic J.
    Maher, Eamonn R.
    Kilby, Mark D.
    FETAL DIAGNOSIS AND THERAPY, 2021, 48 (02) : 112 - 119
  • [50] Prenatal diagnosis of a nonsense mutation in the L1CAM gene resulting in congenital hydrocephalus: A case report and literature review
    Wang, Rongyue
    Chen, Hua
    Wang, Xiaona
    Huang, Shiyuan
    Xie, Ailan
    Wu, Xinmei
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2021, 22 (06)
12345