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CASE REPORT
Year : 2018  |  Volume : 5  |  Issue : 3  |  Page : 236-238

Aicardi syndrome


Department of Radiodiagnosis and Imaging, SKIMS, Srinagar, Jammu and Kashmir, India

Correspondence Address:
Saika Amreen
H. No 28, Humza Colony, Sonawar, Srinagar, Jammu and Kashmir
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/cjhr.cjhr_25_18

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Aicardi syndrome is a rare genetic disease characterized by a characteristic classical trio of neurological clinical abnormalities (spasms), agenesis of the corpus callosum, and ophthalmological abnormalities. Here, we present a case of Aicardi syndrome with complete dysgenesis of the corpus callosum, subependymal periventricular gray matter heterotopia, and a cyst in the interhemispheric fissure. Ophthalmological examination showed bilateral chorioretinal lacunae.


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