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Dear Charmed3862,
I am also the parent of a child who has ACC. He is completely missing his corpus callosum and he was diagnosed with ACC when he was four months old. He is 16 years old now. *edit* I am happy to share the information I have learned about ACC while dealing with my son's medical doctors and specialists. I hope that you and your daughter are doing well. ![]() Sandie Last edited by Jomar; 09-21-2010 at 11:00 PM. Reason: some content removed per NT guidelines |
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Agenesis of the Corpus Callosum (ACC) | General Health Conditions & Rare Disorders |