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What is Aicardi Syndrome? Aicardi Syndrome is a rare genetic disorder characterized by the partial or complete absence of the structure that links the two hemispheres of the brain. The structure that links the two hemispheres of the brain is called the corpus callosum. Aicardi syndrome affects only girls. However, in very rare cases, males with Klinefelter syndrome. Aicardi syndrome usually begins between the ages of 3 and 5 months with infantile spasms, a type of childhood seizure. Aicardi syndrome may be associated with other brain defects such as a smaller than average brain and cavities or gaps in the brain filled with cerebrospinal fluid. Aicardi syndrome was first identified in 1965 by a French neurologist named Dr. Jean Aicardi. Symptoms of Aicardi Syndrome? The most common symptoms of aicardi syndrome are:
Can Aicardi Syndrome be Treated? Currently there is no cure for Aicardi Syndrome. Treatment involves medical management of seizures and programs to help parents and the child cope with developmental delays. How is Aicardi Syndrome diagnosed? If a doctor suspects a child may have Aicardi Syndrome, he will order several tests. Children are diagnosed with Aicardi Syndrome if they meet the following criteria:
However, in rare cases, one of the features, especially lack of development of the corpus callosum, may be missing. If the corpus callosum is developed, the doctor will perform a few more tests. A diagnosis of Aicardi Syndrome is probable if two or more of the following criteria are present:
The doctor will probably perform the following tests:
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