Abstract
A case of Aicardi syndrome is described. The salient features are female sex, agenesis of the corpus callosum, pathognomonic chorioretinopathy, seizures, and mental subnormality. The authors suggest that the incidence of the syndrome may be higher than expected.
Cite
CITATION STYLE
APA
Karagol, U., & Yalaz, K. (1981). Aicardi syndrome. Turkish Journal of Pediatrics, 23(4), 261–268. https://doi.org/10.4103/kjo.kjo_107_22
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