| CASE REPORT |
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| Year : 2018 | Volume
: 5
| Issue : 3 | Page : 236-238 |
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Aicardi syndrome
Saika Amreen, Feroze Shaheen, Tariq Gojwari
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
 Source of Support: None, Conflict of Interest: None  | Check |
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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