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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| 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 |