Familial focal epilepsy with variable foci Title Other Names: FFEVF; Familial partial epilepsy with variable foci Categories: Congenital and Genetic Diseases; Nervous System Diseases This disease is, grouped under: DEPDC5-Related Epilepsy Summary Summary Listen The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.Orpha Number: 98820Disease ...
Epilepsy mental deterioration Finnish type Title News & Events News & Events Listen News NIH Hosts Rare Disease Day Event, Twitter Chat January 24, 2019 Do you have updated information on ...
Myoclonus epilepsy partial seizure Title News & Events News & Events Listen News NIH Hosts Rare Disease Day Event, Twitter Chat January 24, 2019 Do you have updated information on this ...
Juvenile myoclonic epilepsy Información en español Title Other Names: Petit mal, impulsive; JME; EJM; Petit mal, impulsive; JME; EJM; Janz syndrome; Myoclonic epilepsy, juvenile, 1 See More, GARD Information Navigator Try our interactive tool for help finding information, services, experts, financial aid, and more! Summary Summary Listen Juvenile myoclonic epilepsy is an epilepsy syndrome ...
DEPDC5-Related Epilepsy Title Subtypes: Familial focal epilepsy with variable foci Learn More Learn More Listen These resources provide more information about this condition or associated symptoms ...
Myoclonus epilepsy Title Research Research Listen Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn, about medical research and ways to get involved. Clinical Research Resources ClinicalTrials.gov lists trials that are related to Myoclonus epilepsy. Click on the link to go to ClinicalTrials.gov to read ...
Epilepsy occipital calcifications Title Other Names: Epilepsy with bilateral occipital calcifications; Bilateral occipital calcifications with epilepsy; Familial unilateral and bilateral occipital, calcifications and epilepsy; Epilepsy with bilateral occipital calcifications; Bilateral occipital calcifications with epilepsy; Familial unilateral and bilateral occipital calcifications and epilepsy; Celiac ...
Epilepsy with myoclonic-atonic seizures Title Other Names: Myoclonic astatic epilepsy; Doose syndrome; Epilepsy with myoclonic-astatic seizures; Myoclonic astatic epilepsy; Doose syndrome; Epilepsy, with myoclonic-astatic seizures; Epilepsy with myoclono-astatic crisis See More Categories: Congenital and Genetic Diseases; Nervous System Diseases Summary Summary Listen Epilepsy with myoclonic-atonic ...
Benign rolandic epilepsy (BRE) Title Other Names: Benign rolandic epilepsy of childhood (BREC); Benign epilepsy with centro-temporal spikes (BECTS); Benign epilepsy of childhood with centrotemporal, spikes (BECCT) Categories: Nervous System Diseases Summary Summary Listen Benign rolandic epilepsy (BRE) is the most common form of childhood epilepsy. It is referred to as "benign" because most children ...
Progressive myoclonic epilepsy Title Other Names: Familial progressive myoclonic epilepsy Subtypes: Familial encephalopathy with neuroserpin inclusion bodies; Lafora disease; Unverricht-Lundborg, disease Summary Summary Listen Progressive myoclonus epilepsy (PME) refers to a group of inherited conditions involving the central nervous system and representing more than a dozen different diseases ...
