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...

higher in people with epilepsy, especially those with generalized epilepsy. Gene therapy is being studied in some types of epilepsy. Medications that alter...

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

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

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

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,...

LJH; Gripp, K. W.; Amemiya, A. (1993). "KCNT1-Related Epilepsy". KCNT1-Related Epilepsy - GeneReviews® - NCBI Bookshelf. University of Washington, Seattle...

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

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

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

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

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...

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...

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

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

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...

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

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

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

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

EAST syndrome is a syndrome consisting of epilepsy, ataxia (a movement disorder), sensorineural deafness (deafness because of problems with the hearing...

worldwide pioneer in the development of biological bypass surgery and gene therapy for heart failure. North Karelia Central Hospital Urgent Medical Care and...

replacement therapy is in development. The CDKL5 gene is located on the short (p) arm of the X chromosome at position 22. More precisely, the CDKL5 gene is located...

a carrier. The ASAH1 gene is also known to cause a condition called spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME). Farber disease...

Sleep-related hypermotor epilepsy (SHE), previously known as nocturnal frontal lobe epilepsy, is a form of focal epilepsy characterized by seizures which...