An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family

Abstract Background Craniosynostosis, defined as premature fusion of one or more cranial sutures, affects approximately 1 in every 2000–2500 live births. Sagittal craniosynostosis (CS), the most prevalent form of isolated craniosynostosis, is caused by interplay between genetic and perinatal environ...

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Principais autores:	Jin Xu, Qing Yan, Chengcheng Song, Jingjia Liang, Liang Zhao, Xin Zhang, Zhenkun Weng, Cheng Xu, Qian Liu, Shuqin Xu, Lu Pang, Liye Zhang, Yuan Sun, Gang Wang, Aihua Gu
Formato:	Artigo
Idioma:	Inglês
Publicado:	BMC 2021-06-01
Series:	Hereditas
Assuntos:	Sagittal craniosynostosis Axin2 Perinatal risk factors Mutation Monochorionic diamniotic twin
Acceso en liña:	https://doi.org/10.1186/s41065-021-00182-0
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