Experts Recommend 1-2 mg Folic Acid for Pregnant People with Epilepsy
A recent study surveyed international experts to understand their recommendations for folic acid supplementation in pregnant people with epilepsy.
This hub covers pediatric epilepsy in infants, kids, and teens, including diagnosis, syndromes, development, school plans, and safety. New studies translated into clear takeaways for parents.
Usually when two appropriate medications haven’t controlled seizures.
Many families benefit and it depends on seizure frequency, medications, and learning needs.
Often yes, with smart precautions. Ask your neurologist or epileptologist about your child’s specific risks.
Clusters, prolonged seizures, breathing trouble, new weakness, or major regression.
A recent study surveyed international experts to understand their recommendations for folic acid supplementation in pregnant people with epilepsy.
This study looked at how children aged 8 to 17 experience long-term video-electroencephalography monitoring (LTVEM), a procedure used to diagnose epilepsy when medications donβt work.
In a recent study, researchers looked at how well neurologists in the United States are following new guidelines for genetic testing and counseling for patients with unexplained epilepsy.
A recent study looked at how EEG (electroencephalogram) results can help predict the chances of having more seizures after someone experiences their first unprovoked seizure.
This study looked at how schools can support children and teenagers with chronic health conditions, like epilepsy, asthma, and ADHD.
Researchers studied a new tool called PredictMed-CDSS, which is designed to help predict the likelihood of developing neuromuscular hip dysplasia (NHD) in children with cerebral palsy (CP).
This study looked at children with a specific genetic condition called SYNGAP1-related developmental and epileptic encephalopathy (DEE), which causes severe developmental issues and epilepsy.
This study looked at 37 children who had changes in a specific part of their DNA called the 15q11.2 region.
This study looked at a rare genetic disorder called spinocerebellar ataxia type 13 (SCAR13) in two families from Pakistan.