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Singh P, Goraya JS, Saggar K, Ahluwalia A
Correspondence: Dr Paramdeep Singh, email@example.com
Aicardi syndrome is a rare neurodevelopmental disease characterised by congenital chorioretinal lacunae, corpus callosum dysgenesis, seizures, polymicrogyria, cerebral callosum, chorioretinopathy and electroencephalogram abnormality. We present a case of Aicardi syndrome with callosal hypogenesis in a 4.5-month-old baby who presented with infantile spasms. Ophthalmoscopy revealed chorioretinal lacunae. The clinical and magnetic resonance imaging features were diagnostic of Aicardi syndrome.
Keywords: Aicardi, callosal dysgenesis, chorioretinal lacunae, infantile spasms
Singapore Med J 2012; 53(7):e153–e155