Differential diagnosis of syndromic craniosynostosis: a case series

PURPOSE: Syndromic craniosynostosis is a rare genetic disease caused by premature fusion of one or multiple cranial sutures combined with malformations of other organs. The aim of this publication is to investigate sonographic signs of different syndromic craniosynostoses and associated malformation...

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Detalles Bibliográficos
Autores principales: Casteleyn, Tamara, Horn, Denise, Henrich, Wolfgang, Verlohren, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Maternal-Fetal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300495/
https://www.ncbi.nlm.nih.gov/pubmed/34633507
http://dx.doi.org/10.1007/s00404-021-06263-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300495/
https://www.ncbi.nlm.nih.gov/pubmed/34633507
http://dx.doi.org/10.1007/s00404-021-06263-9

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