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Doctors closer to a breakthrough in infant epilepsy

Wednesday 18th January 2012

A team of researchers in Australia have moved a step closer to figuring out why epileptic seizures occur in infants.

The doctors have found a new gene, known as PRRT2, which is believed to cause the protein linked to the condition to form incorrectly. The team at the University of Melbourne recognised that benign familial infantile epilepsy (BFIE), better known as infantile seizures, can be passed down through families.

Researchers found that families that had BFIE also contained the PRRT2 gene resulting in it being passed down to their offspring. However, despite the molecule being pinpointed doctors still alluded to how it functions or how it changes to cause the seizures in infants.

BFIE is a condition that occurs in children who are developing normally and the seizures tend to occur when the infant is between the ages of six months and two years. Whilst the strain of the disease is a rare one the Australian team still considers it to be serious and if it is left to mutate within an infant it can cause an unusual movement disorder known as Paroxysmal Kinesigenic Choreoathetosis.

Professor Ingrid Scheffer, chair of paediatric neurology research said: "The findings will help families understand why their baby has seizures and provides reassurance that the baby will grow out of the seizures and not have long term problems. It will also help with early diagnosis and appropriate treatment of the movement disorder."

In the UK an epilepsy society is finding ways to help children get through having the condition at a young age. Young Epilepsy has introduced a "seizure diary" for children to fill in so that they can chart their progress but in a "fun way". The booklet is also essential for doctors so that they can monitor a child's development at combating the illness.

Gill Gallagher, Young Epilepsy's childhood epilepsy information service manager, said: "We wanted something a child could take to school and which would look and feel like an ordinary diary, we're delighted with the amazing support we've had from children’s authors and illustrators."

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Written by Mathew HortonADNFCR-1780-ID-801268459-ADNFCR

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