Neurodevelopmental disorders and anti-epileptic treatment in a patient with a SATB1 mutation: A case report

SATB1 variants causing developmental delay with dysmorphic facies and dental anomalies have been reported in a small cohort. Most patients present epilepsy as a main clinical feature in neurodevelopmental disorders; however, its treatment is unknown. Here, we present a Chinese patient with a de novo...

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Detalles Bibliográficos
Autores principales: Yu, Ying, Li, Cuiyun, Li, Wei, Chen, Liting, Wang, Dan, Wang, Jie, Wang, Jian, Yao, Ruen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479181/
https://www.ncbi.nlm.nih.gov/pubmed/36120649
http://dx.doi.org/10.3389/fped.2022.931667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479181/
https://www.ncbi.nlm.nih.gov/pubmed/36120649
http://dx.doi.org/10.3389/fped.2022.931667

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