Refractory Seizures with Global Developmental Delay: A Rare Cause
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Abstract
Aicardi syndrome is a genetic disorder characterized by the triad of infantile spasm in flexion, callosal agenesis and ocular abnormalities (chorioretinal lacunae, coloboma of optic disc). We report a typical case of Aicardi syndrome with all the classical features.
References
1.
Phillips H, Carter A, KENNEDY Jr J, ROSMAN N, OConnor J
. Aicardi's syndrome; radiologic manifestations. Radiology. 1978; 127(2):453-5.
DOI: 10.1148/127.2.453.
View
2.
Singhi P, Gupta A, Agarwal A
. Aicardi syndrome. Indian Pediatr. 1991; 28(12):1513-6.
View
3.
Ropers H, Zuffardi O, Bianchi E, TIEPOLO L
. Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation. Hum Genet. 1982; 61(4):364-8.
DOI: 10.1007/BF00276602.
View
4.
Font R, Marines H, Cartwright Jr J, Bauserman S
. Aicardi syndrome. A clinicopathologic case report including electron microscopic observations. Ophthalmology. 1991; 98(11):1727-31.
DOI: 10.1016/s0161-6420(91)32059-1.
View
5.
Hopkins I, Humphrey I, Keith C, Susman M, Webb G, TURNER E
. The Aicardi syndrome in a 47, XXY male. Aust Paediatr J. 1979; 15(4):278-80.
DOI: 10.1111/j.1440-1754.1979.tb01246.x.
View