Autism Can Be Inherited From Relatives With Epilepsy, Study Shows

Studies can now provide supportive evidence on the risks of birthing a child with autism spectrum disorder, and that it could stemmed from one's gene pool. The American Academy of Neurology recently featured in its online medical journal that a relative with epilepsy could be a direct link to developing autism in children, the Science Daily reported.

Dr. Heléne E.K. Sundelin, MD, who directed the study together with University Hospital in Linköping, Sweden, said that the group's studies produced verified results linking both conditions. She adds that the study was geared in particular to siblings and offspring of persons having epilepsy in relation to determining the probable risk of autism with their relatives.

A six-year follow up of the study revealed 1,381 participants with epilepsy as well as 700 people without epilepsy were determined as having autism. The study went on to conclude that people with epilepsy held increased risk to have autism (1.6%), with greatest risk identified in people diagnosed with epilepsy during childhood (5.2%).

In related news, Sundelin's team also found out of a 63% risk of developing autism in children who have siblings or parents with epilepsy. Mothers with epilepsy have also been found to pose a 91% icreased risk for their offspring to have autism spectrum disorder, with a 38% increased risk if the father has epilepsy, in a UPI post.

According to the researchers, as stated in their study, individuals with epilepsy exhibited a high potential risk of developing autism spectrum disorder, especially if the former was identified during early childhood. The team is still looking for further proof in understanding the important role that genetics play in the risks associated with epilepsy and autism in children.

However, they hold onto this latest development. "The goal is to find out more about how these two diseases may be linked so that treatments may be developed that will target both conditions," added Sundelin.