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Xp22 GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia [Agenesis of corpus callosum] [Eyes] Aicardi syndrome *Gene map locus Xp22 AIC Agenesis of corpus callosum with chorioretinal abnormality Corpus callosum agenesis with chorioretinal abnormality [Clinical features: agenesis of corpus callosum; mental retardation; infantile spasms; chorioretinal abnormality] [Inheritance: X-linked dominant] |
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Aicardi syndrome |
Aicardi syndrome |
A Female Child with Corpus Callosum agenesis and infantile spasm |
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Neuroneonatology |
Neuroneonatology |
Oman Medical Journal |
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A Female Child with Corpus Callosum agenesis and infantile spasm |
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Oman Medical Journal |
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Edited by Aldo Campana,
August 21, 2012
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