Faster access than browser!Similarities between Epilepsy and Epilepsy syndromes
Epilepsy and Epilepsy syndromes have 24 things in common (in Unionpedia): Absence seizure, Angelman syndrome, Anticonvulsant, Aura (symptom), Autism spectrum, Autosomal dominant nocturnal frontal lobe epilepsy, Childhood absence epilepsy, Down syndrome, Dravet syndrome, Electroencephalography, Epilepsy surgery, Epileptic seizure, Epileptic spasms, Gene, Generalised tonic-clonic seizure, Hippocampus, Inheritance, Juvenile myoclonic epilepsy, Lennox–Gastaut syndrome, Management of drug-resistant epilepsy, Photosensitive epilepsy, Reflex seizure, Rolandic epilepsy, Temporal lobe epilepsy.
Absence seizure
Absence seizures are one of several kinds of generalized seizures.
Absence seizure and Epilepsy · Absence seizure and Epilepsy syndromes ·
Angelman syndrome
Angelman syndrome (AS) is a genetic disorder that mainly affects the nervous system.
Angelman syndrome and Epilepsy · Angelman syndrome and Epilepsy syndromes ·
Anticonvulsant
Anticonvulsants (also commonly known as antiepileptic drugs or as antiseizure drugs) are a diverse group of pharmacological agents used in the treatment of epileptic seizures.
Anticonvulsant and Epilepsy · Anticonvulsant and Epilepsy syndromes ·
Aura (symptom)
An aura is a perceptual disturbance experienced by some with migraines or seizures before either the headache or seizure begins.
Aura (symptom) and Epilepsy · Aura (symptom) and Epilepsy syndromes ·
Autism spectrum
Autism spectrum, also known as autism spectrum disorder (ASD), is a range of conditions classified as neurodevelopmental disorders.
Autism spectrum and Epilepsy · Autism spectrum and Epilepsy syndromes ·
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is an epileptic disorder that causes frequent violent seizures during sleep.
Autosomal dominant nocturnal frontal lobe epilepsy and Epilepsy · Autosomal dominant nocturnal frontal lobe epilepsy and Epilepsy syndromes ·
Childhood absence epilepsy
Childhood absence epilepsy (CAE), also known as pyknolepsy, is an idiopathic generalized epilepsy which occurs in otherwise normal children.
Childhood absence epilepsy and Epilepsy · Childhood absence epilepsy and Epilepsy syndromes ·
Down syndrome
Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21.
Down syndrome and Epilepsy · Down syndrome and Epilepsy syndromes ·
Dravet syndrome
Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a type of epilepsy with seizures that are often triggered by hot temperatures or fever.
Dravet syndrome and Epilepsy · Dravet syndrome and Epilepsy syndromes ·
Electroencephalography
Electroencephalography (EEG) is an electrophysiological monitoring method to record electrical activity of the brain.
Electroencephalography and Epilepsy · Electroencephalography and Epilepsy syndromes ·
Epilepsy surgery
Epilepsy surgery involves a neurosurgical procedure where an area of the brain involved in seizures is either resected, disconnected or stimulated.
Epilepsy and Epilepsy surgery · Epilepsy surgery and Epilepsy syndromes ·
Epileptic seizure
An epileptic seizure is a brief episode of signs or symptoms due to abnormally excessive or synchronous neuronal activity in the brain.
Epilepsy and Epileptic seizure · Epilepsy syndromes and Epileptic seizure ·
Epileptic spasms
Epileptic spasms, also known as infantile spasms, juvenile spasms, or West syndrome is an uncommon-to-rare epileptic disorder in infants, children and adults.
Epilepsy and Epileptic spasms · Epilepsy syndromes and Epileptic spasms ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Epilepsy and Gene · Epilepsy syndromes and Gene ·
Generalised tonic-clonic seizure
A generalized tonic–clonic seizure (formerly known as a grand mal seizure) is a type of generalized seizure that affects the entire brain.
Epilepsy and Generalised tonic-clonic seizure · Epilepsy syndromes and Generalised tonic-clonic seizure ·
Hippocampus
The hippocampus (named after its resemblance to the seahorse, from the Greek ἱππόκαμπος, "seahorse" from ἵππος hippos, "horse" and κάμπος kampos, "sea monster") is a major component of the brains of humans and other vertebrates.
Epilepsy and Hippocampus · Epilepsy syndromes and Hippocampus ·
Inheritance
Inheritance is the practice of passing on property, titles, debts, rights, and obligations upon the death of an individual.
Epilepsy and Inheritance · Epilepsy syndromes and Inheritance ·
Juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME), also known as Janz syndrome, is a fairly common form of idiopathic generalized epilepsy, representing 5-10% of all epilepsy cases.
Epilepsy and Juvenile myoclonic epilepsy · Epilepsy syndromes and Juvenile myoclonic epilepsy ·
Lennox–Gastaut syndrome
Lennox–Gastaut syndrome (LGS) is a childhood-onset epilepsy that most often appears between the second and sixth year of life.
Epilepsy and Lennox–Gastaut syndrome · Epilepsy syndromes and Lennox–Gastaut syndrome ·
Management of drug-resistant epilepsy
Drug-resistant epilepsy (DRE), also known as refractory epilepsy or pharmacoresistant epilepsy, is defined as failure of adequate trials of two tolerated and appropriately chosen and used antiepileptic drugs (AED schedules) (whether as monotherapies or in combination) to achieve sustained seizure freedom.
Epilepsy and Management of drug-resistant epilepsy · Epilepsy syndromes and Management of drug-resistant epilepsy ·
Photosensitive epilepsy
Photosensitive epilepsy (PSE) is a form of epilepsy in which seizures are triggered by visual stimuli that form patterns in time or space, such as flashing lights; bold, regular patterns; or regular moving patterns.
Epilepsy and Photosensitive epilepsy · Epilepsy syndromes and Photosensitive epilepsy ·
Reflex seizure
Reflex seizures are epileptic seizures that are consistently induced by a specific stimulus or trigger making them distinct from normal eplipetic seizures, which are usually unprovoked.
Epilepsy and Reflex seizure · Epilepsy syndromes and Reflex seizure ·
Rolandic epilepsy
Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood.
Epilepsy and Rolandic epilepsy · Epilepsy syndromes and Rolandic epilepsy ·
Temporal lobe epilepsy
Temporal lobe epilepsy (TLE) is a chronic disorder of the nervous system characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes.
Epilepsy and Temporal lobe epilepsy · Epilepsy syndromes and Temporal lobe epilepsy ·
The list above answers the following questions
- What Epilepsy and Epilepsy syndromes have in common
- What are the similarities between Epilepsy and Epilepsy syndromes
Epilepsy and Epilepsy syndromes Comparison
Epilepsy has 244 relations, while Epilepsy syndromes has 59. As they have in common 24, the Jaccard index is 7.92% = 24 / (244 + 59).
References
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