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Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy–Walker malformation
BACKGROUND: Posterior fossa malformations are among the most diagnosed central nervous system (CNS) anomalies detected by ultrasound (US) in prenatal age. We identified the pathogenic gene mutation in a male fetus of 17 weeks of gestation with US suspicion of familial Dandy–Walker spectrum malformat...
Autores principales: | Traversa, Alice, Bernardo, Silvia, Paiardini, Alessandro, Giovannetti, Agnese, Marchionni, Enrica, Genovesi, Maria Luce, Guadagnolo, Daniele, Torres, Barbara, Paolacci, Stefano, Bernardini, Laura, Mazza, Tommaso, Carella, Massimo, Caputo, Viviana, Pizzuti, Antonio |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978243/ https://www.ncbi.nlm.nih.gov/pubmed/31756055 http://dx.doi.org/10.1002/mgg3.1054 |
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