Improving Access to Genetic Testing for Unexplained Epilepsy
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.
Pediatric epilepsy research translated for parents into normal language, including summaries about diagnosis, treatments, school, safety, and safety.
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.
Researchers studied how often unreported information about genetic changes, known as variants of uncertain significance (VUS), is found in children with epilepsy.
This study looked at children with a condition called acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), which can occur after infections.