Gene therapy is being studied for some forms of epilepsy. It relies on viral or non-viral vectors to deliver DNA or RNA to target brain areas where seizures...

current. Gene therapy for color blindness Gene therapy for epilepsy Gene therapy for osteoarthritis Gene therapy in Parkinson's disease Gene therapy of the...

therapy gene therapy for color blindness gene therapy for epilepsy gene therapy for osteoarthritis gene therapy in Parkinson's disease gene therapy of the...

recommended if there is any doubt. Due to drug-refractory epilepsy in DS, many other therapies are being explored to prolong the life expectancy of patients...

Gene therapy for osteoarthritis is the application of gene therapy to treat osteoarthritis (OA). Unlike pharmacological treatments which are administered...

genes: gene therapy gene therapy for epilepsy gene therapy for osteoarthritis gene therapy for color blindness gene therapy of the human retina gene therapy...

factors are higher in epilepsy patients, especially those with generalized epilepsy. Gene therapy is being studied in some types of epilepsy. Medications that...

low-carbohydrate dietary therapy that in conventional medicine is used mainly to treat hard-to-control (refractory) epilepsy in children. The diet forces...

Epilepsy Therapy Project. "Absence Seizures". Epilepsy Foundation. Retrieved 8 May 2013. V. Crunelli, N. Leresche Childhood absence epilepsy: genes,...

lacking. Two promising areas include gene therapy, and seizure detection and seizure prediction. Gene therapy for epilepsy consists of employing vectors to...

Progressive Myoclonic Epilepsies (PME) are a rare group of inherited neurodegenerative diseases characterized by myoclonus, resistance to treatment, and...

his own son, James Edwin West (1840–1860). Other names for it are "generalized flexion epilepsy", "infantile epileptic encephalopathy", "infantile myoclonic...

cortical dysplasia is a common cause of intractable epilepsy in children and is a frequent cause of epilepsy in adults. There are three types of FCD with subtypes...

responsible for the disease occurs in the dystrophin gene. CRISPR has been used to correct for this. Similarly, for Dravet syndrome, which is an epilepsy disorder...

MERRF syndrome (or myoclonic epilepsy with ragged red fibers) is a mitochondrial disease. It is extremely rare, and has varying degrees of expressivity...

Epilepsy-intellectual disability in females also known as PCDH19 gene-related epilepsy or epileptic encephalopathy, early infantile, 9 (EIEE9), is a rare...

health defects including Hirschsprung disease, intellectual disability, epilepsy, delayed growth and motor development, congenital heart disease, genitourinary...

Myoclonic astatic epilepsy (MAE), also known as myoclonic atonic epilepsy or Doose syndrome, and renamed "Epilepsy with myoclonic-atonic seizures" in the...

Cognitive behavioral therapy for insomnia (CBT-I) is a technique for treating insomnia without (or alongside) medications. Insomnia is a common problem...

caused by pathogenic variants in the gene CDKL5. The symptoms of CDD include early infantile onset refractory epilepsy; hypotonia; developmental, intellectual...

Characteristic facial appearance (but not in all cases). A history of epilepsy and an abnormal EEG tracing. A happy disposition with frequent laughter...

generalized EEG pattern seen particularly during absence epilepsy, also known as ‘petit mal’ epilepsy. The basic mechanisms underlying these patterns are complex...

with SLC13A5 Epilepsy require an accurate diagnosis to receive proper treatment, particularly with the precision therapy in development for this disease...

myoclonic epilepsy, it is a second-line therapy, reserved for when the valproates or lamotrigine do not work and when the other second-line therapy, acetazolamide...

Pennsylvania to develop an ASO under a program focused on developing new therapies for Epilepsy and Neuro-Developmental Disorders (ENDD). The MIND Institute at...

disability, epilepsy, musculoskeletal anomalies, altered pain perception, ataxia, hypotonia, nystagmus, and cerebellar atrophy. The earliest sign for TRPM3-related...

PRICKLE1-related progressive myoclonus epilepsy with ataxia is a very rare genetic disorder which is characterized by myoclonic epilepsy and ataxia. Ataxia is usually...

terms of enrollment. KYS has an Epilepsy Center (Epilepsiakeskus) that provides diagnostics and treatment for severe epilepsy in both adults and children...

schizophrenia. Gene therapy is the delivery of nucleic acid as a treatment for a disorder. In translational neuroscience, gene therapy is the delivery...

syndrome frequently co-occurs with attention deficit hyperactivity disorder, epilepsy and intellectual disability, and research indicates that autistic people...