New Genetic Findings May Improve Care In RHOBTB2 Disorders
This study looked at RHOBTB2-related disorders, which are rare genetic conditions linked to developmental problems, epilepsy, and movement symptoms.
This study looked at RHOBTB2-related disorders, which are rare genetic conditions linked to developmental problems, epilepsy, and movement symptoms.
This study looked at tubulinopathies, a group of neurodevelopmental disorders caused by changes in tubulin-related genes and microtubule-associated proteins.
This study looked at whether outside factors, not just the gene change itself, were linked with development in people with genetic neurodevelopmental disorders (NDDs).
This study followed 665 adults with drug-resistant focal epilepsy after an anti-seizure medicine was added or substituted.
This article is a conference summary, not a single clinical trial.
This paper is a review, not a new experiment.
This study looked at everyday functioning in children and teens with drug-resistant epilepsy who had palliative epilepsy surgery.
This paper was a systematic review, meaning the researchers gathered and summarized published reports about a rare genetic condition called ring chromosome 20 and the epilepsy linked to it.
This pilot study looked at whether circadian rest-activity rhythms and sleep parameters differ in adolescents with juvenile myoclonic epilepsy (JME) compared with healthy teens.