Examples of 'myoclonic epilepsy' in a sentence
Meaning of "myoclonic epilepsy"
myoclonic epilepsy: Myoclonic epilepsy is a neurological disorder characterized by brief, involuntary muscle jerks or twitches. It is a type of epilepsy that can cause sudden and sporadic muscle contractions. These episodes can vary in severity and frequency, and they may or may not be accompanied by other seizure symptoms like loss of consciousness
How to use "myoclonic epilepsy" in a sentence
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myoclonic epilepsy
Myoclonic epilepsy with ragged red fibres.
The cause of juvenile myoclonic epilepsy is not known.
Lafora disease is fatal intractable progressive myoclonic epilepsy.
Juvenile myoclonic epilepsy is sometimes linked with lack of compliance with treatment.
Topiramate for juvenile myoclonic epilepsy.
The seizures of juvenile myoclonic epilepsy often occur when people first awaken in the morning.
The majority of patients presented with juvenile myoclonic epilepsy.
This syndrome is characterised by myoclonic epilepsy with generalised spasticity and intellectual deficit.
We find such conditions in cases of catalepsy and also in myoclonic epilepsy.
Myoclonic epilepsy in Rhodesian ridgebacks.
Geneticists are inclined to think about the mechanism of inheritance of polygenic myoclonic epilepsy.
The exact cause of Juvenile Myoclonic Epilepsy remains unknown.
Then the neuro doc appologized and said that diagnosis was a mistake, that I had Myoclonic Epilepsy.
JME is a form of myoclonic epilepsy - generalized epilepsy with myoclonic seizures occurring.
Mutations in this gene are associated with progressive myoclonic epilepsy type 5.
See also
Myoclonic epilepsy and ragged-red fibers.
Mutations in EFHC1 have been linked to juvenile myoclonic epilepsy.
Juvenile myoclonic epilepsy is responsible for 7% of cases of epilepsy.
Dravet syndrome is also known as the severe myoclonic epilepsy in infancy ( SMEI ).
Juvenile myoclonic epilepsy ( including generalised tonic-clonic seizures on awakening ).
Mutations in the MT-TK gene are associated with myoclonic epilepsy and ragged-red fiber disease MERRF.
Severe myoclonic epilepsy in infancy ( Dravet syndrome ).
Neurodevelopment in new-onset juvenile myoclonic epilepsy over the first 2 years.
Juvenile myoclonic epilepsy ( JME ) is a type of epilepsy, which begins in childhood or adolescence.
It is also known as severe myoclonic epilepsy of infancy ( SMEI ).
Efficient in treating focal seizures, Lennox-Gastaut syndrome, West syndrome, and juvenile myoclonic epilepsy.
In 3-5 % of cases of juvenile myoclonic epilepsy occurs only with the presence of myoclonic seizures.
EP1731149 discloses the use of brivaracetam for the prevention or treatment of progressive myoclonic epilepsy.
Pure epilepsies due to single gene disorder ( e . g. severe myoclonic epilepsy of childhood or Dravet syndrome ).
Juvenile myoclonic epilepsy 25 years after seizure onset, a population-based study.
Charlotte Dravet first described severe myoclonic epilepsy of infancy in France, 1978.
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