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

• Main Authors: Ying Yu (Author), Cuiyun Li (Author), Wei Li (Author), Liting Chen (Author), Dan Wang (Author), Jie Wang (Author), Jian Wang (Author), Ruen Yao (Author)
• Format: Book
• Published: Frontiers Media S.A., 2022-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...