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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2021
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| 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 |