Cargando…
Clinical characterization of epilepsy in children with chromosomal aberration 47, XXY
OBJECTIVE: The phenotype of the chromosomal aberration 47, XXY exhibits considerable heterogenicity. In addition, epilepsy is extremely uncommon in individuals with this chromosomal disorder. As a result, the clinical characteristics of epilepsy in these patients remain poorly understood. METHODS: C...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2023
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454333/ https://www.ncbi.nlm.nih.gov/pubmed/37479950 http://dx.doi.org/10.1002/brb3.3178 |