Neurodevelopmental disorders and anti-epileptic treatment in a patient with a SATB1 mutation: A case report.
Front Pediatr
; 10: 931667, 2022.
Article
in En
| MEDLINE
| ID: mdl-36120649
ABSTRACT
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 truncating variation in SATB1 who presented with mild developmental delay. We disclose the detailed anti-epileptic pharmacological treatment that enabled a favorable outcome. Our study provides important information that may aid clinicians in the prognosis and treatment of rare neurological developmental disorders caused by gene mutations.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Prognostic_studies
Language:
En
Journal:
Front Pediatr
Year:
2022
Document type:
Article
Affiliation country:
China