Aicardi syndrome typically triggers youth seizure (intantile convulsions), eye problem or sores of the retina, and metal retardation. Aicardi Syndrome is likewise connected to microcephaly, a brain flaw; microgyria, where bumps inside the brain tend to be narrow; or porecenphalic cysts, a brain condition triggering fluids to fill the spaces in the brain.
It is kids, in between 3 to 5 months, who are most typically branded with Aicardi Syndrome. Infantile convulsions at this age triggers neural synapses to close, thus hindering the children’ brain advancement. A baby affected with the syndrome might likewise experience hold-ups in advancement.
The medical professional thought the syndrome was triggered by a shortage in the woman chromosome (X). The condition just impacts bulk of female babies, although there is one reported case of an infant kid identified with the syndrome.
There is presently no remedy for Aicardi Syndrome. The life span for a baby affected with Aicardi syndrome is reliant on how extreme the condition is.
The National Institute of Neurological Disorder and Stroke (NINDS) is presently doing a substantial research study on Aircardi Syndrome. The goal is to figure out and even more comprehend the genes included to be able to discover much better treatment, avoidance and eventually, a treatment for this condition.
Aicardi syndrome frequently triggers youth seizure (intantile convulsions), eye problem or sores of the retina, and metal retardation. Aicardi Syndrome is likewise connected to microcephaly, a brain problem; microgyria, where bumps inside the brain tend to be narrow; or porecenphalic cysts, a brain condition triggering fluids to fill the spaces in the brain. It is kids, in between 3 to 5 months, who are most frequently branded with Aicardi Syndrome. There is presently no remedy for Aicardi Syndrome.