Missed diagnosis of lissencephaly after prenatal diagnosis: A case report

Lissencephaly (LIS) is a rare and serious cortical malformation characterized by a smooth or nearly smooth brain surface. With the progress of molecular genetics, platelet-activating factor acetylhydrolase brain isoform Ib is the most frequent type during the fetal period. Here, we report an infant...

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Detalles Bibliográficos
Autores principales: Liu, Mengna, Liu, Xiao, Wu, Jiebin, Sha, Jing, Zhai, Jingfang, Zhang, Bei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936017/
https://www.ncbi.nlm.nih.gov/pubmed/36800618
http://dx.doi.org/10.1097/MD.0000000000033014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936017/
https://www.ncbi.nlm.nih.gov/pubmed/36800618
http://dx.doi.org/10.1097/MD.0000000000033014

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