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Ocular features in Aicardi syndrome: A case report

Aicardi syndrome is a genetic malformation syndrome with a triad of dysgenesis or agenesis of the corpus callosum, distinctive chorioretinal lacunae and infantile spasms. It is a rare developmental disorder first described in 1965. The disease affects 1 in 100,000 live births. PATIENT CONCERNS: We d...

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Detalles Bibliográficos
Autores principales:	Sirek, Sebastian, Filipek, Erita, Wójcik–Niklewska, Bogumiła, Pojda-Wilczek, Dorota, Mrukwa-Kominek, Ewa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	5800
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750684/ https://www.ncbi.nlm.nih.gov/pubmed/36626525 http://dx.doi.org/10.1097/MD.0000000000031950

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