Aicardi Syndrome: An Epidemiologic and Clinical Study in Norway

Abstract Background Aicardi syndrome is a rare neurodevelopmental disorder. The main diagnostic features are agenesis of corpus callosum, chorioretinal lacunae, and infantile spasms. The outcome is in general severe, with poor cognitive development and difficult-to-treat epilepsy. The aim of this st...

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Veröffentlicht in:	Pediatric neurology 2015-02, Vol.52 (2), p.182-186.e3
Hauptverfasser:	Lund, Caroline, MD, Bjørnvold, Marit, MD, PhD, Tuft, Mia, MS, Kostov, Hrisimir, MD, Røsby, Oddveig, MD, PhD, Selmer, Kaja K., MD, PhD
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Agenesis of Corpus Callosum - complications Agenesis of Corpus Callosum - pathology Aicardi syndrome Aicardi Syndrome - diagnosis Aicardi Syndrome - epidemiology Child Child, Preschool epilepsy Female Humans Infant Infant, Newborn Neurology Norway - epidemiology Pediatrics prevalence rare disease Young Adult
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