作者
Julia Wallmeier, Diana Frank, Amelia Shoemark, Tabea Nöthe-Menchen, Sandra Cindric, Heike Olbrich, Niki T Loges, Isabella Aprea, Gerard W Dougherty, Petra Pennekamp, Thomas Kaiser, Hannah M Mitchison, Claire Hogg, Siobhán B Carr, Maimoona A Zariwala, Thomas Ferkol, Margaret W Leigh, Stephanie D Davis, Jeffrey Atkinson, Susan K Dutcher, Michael R Knowles, Holger Thiele, Janine Altmüller, Henrike Krenz, Marius Wöste, Angela Brentrup, Frank Ahrens, Christian Vogelberg, Deborah J Morris-Rosendahl, Heymut Omran
发表日期
2019/11/7
期刊
The American Journal of Human Genetics
卷号
105
期号
5
页码范围
1030-1039
出版商
Elsevier
简介
Hydrocephalus is one of the most prevalent form of developmental central nervous system (CNS) malformations. Cerebrospinal fluid (CSF) flow depends on both heartbeat and body movement. Furthermore, it has been shown that CSF flow within and across brain ventricles depends on cilia motility of the ependymal cells lining the brain ventricles, which play a crucial role to maintain patency of the narrow sites of CSF passage during brain formation in mice. Using whole-exome and whole-genome sequencing, we identified an autosomal-dominant cause of a distinct motile ciliopathy related to defective ciliogenesis of the ependymal cilia in six individuals. Heterozygous de novo mutations in FOXJ1, which encodes a well-known member of the forkhead transcription factors important for ciliogenesis of motile cilia, cause a motile ciliopathy that is characterized by hydrocephalus internus, chronic destructive airway …
引用总数
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