Aicardi syndrome in a 7-month-old girl with tonic seizures and skeletal defects: A case report

INTRODUCTION: and importance: Aicardi syndrome (AS) is a rare genetic syndrome characterized by a triad of features: agenesis or hypogenesis of corpus callosum, chorioretinal lacunae, and infantile spasms, along with other neurodevelopmental, ocular, craniofacial, gastrointestinal, and musculoskelet...

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Detalles Bibliográficos
Autores principales: Saado, Saeed, Bara, Albaraa, Abdallah, Yazane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181190/
https://www.ncbi.nlm.nih.gov/pubmed/34136214
http://dx.doi.org/10.1016/j.amsu.2021.102447

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181190/
https://www.ncbi.nlm.nih.gov/pubmed/34136214
http://dx.doi.org/10.1016/j.amsu.2021.102447

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