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Xp22 GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia [Agenesis of corpus callosum] 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 |
Aicardi syndrome with Dandy-Walker malformation |
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eMedicine |
Eyeatlas |
Indian Pediatrics |
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