Examples of 'dravet syndrome' in a sentence
Meaning of "dravet syndrome"
Dravet syndrome, also known as severe myoclonic epilepsy of infancy (SMEI), is a rare and severe form of epilepsy that usually begins in infancy or early childhood. It is characterized by frequent and prolonged seizures, developmental delays, and other neurological and cognitive impairments
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- An autosomal-dominant genetic disorder that causes a catastrophic form of epilepsy, usually beginning in infancy, with prolonged seizures that are often triggered by high temperatures or fever.
How to use "dravet syndrome" in a sentence
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dravet syndrome
Dravet syndrome presents differently in each patient.
Indicated for the treatment of Dravet syndrome.
Dravet syndrome is a severe form of epilepsy.
Method for the treatment of Dravet syndrome.
Dravet syndrome is a very rare condition caused by a genetic mutation.
Sudden unexpected death in a mouse model of Dravet syndrome.
Dravet syndrome is a rare and catastrophic form of epilepsy beginning in childhood.
It was the first drug approved to treat Dravet syndrome.
Dravet syndrome is also associated with sleep disorders including somnolence and insomnia.
This is particularly true for children with Dravet syndrome.
Dravet Syndrome is a severe epileptic encephalopathy starting in the first year of life.
It is known that patients with Dravet Syndrome commonly experience photosensitive or induced seizures.
Dravet Syndrome is a rare and catastrophic form of intractable epilepsy that begins in infancy.
Clinical trials have studied the use of fenfluramine in patients with Dravet syndrome.
People with Dravet syndrome often have problems with behavior and teaching.
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Since her retirement she has focused her activities on the Dravet syndrome.
Cannabis oil is also thought to treat Dravet syndrome and relieve headaches and migraines.
Little is known about the long term prognosis of people with Dravet syndrome.
Seizures associated with Dravet Syndrome are typically resistant to conventional treatments.
Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome.
Children with Dravet Syndrome are likely to experience multiple seizures per day.
Much remains to be understood about the causes of Dravet Syndrome and research is ongoing.
Dravet syndrome causes ongoing seizures, cognitive problems and risk of early death.
People affected by Dravet syndrome.
Dravet syndrome is also known as the severe myoclonic epilepsy in infancy ( SMEI ).
There are a number of genetic mutations that are indicative of Dravet Syndrome.
That was before Dravet Syndrome entered their lives.
They hope the discovery will help those with Dravet Syndrome.
Also, many children with Dravet syndrome have seizures triggered by light.
These vectors will be evaluated in a mouse model designed by the Dravet Syndrome Foundation.
For many patients, Dravet syndrome severely impacts mobility and slows cognitive function.
He was diagnosed with Dravet Syndrome.
Dravet Syndrome is under-diagnosed.
Epidiolex in Dravet syndrome.
Currently, there aren no medications on the market specifically to treat Dravet syndrome.
Even with treatment, people with LGS or Dravet syndrome may continue to experience persistent seizures.
The fast-track designation was granted for Dravet syndrome.
Of particular concern, children with Dravet Syndrome are particularly susceptible to episodes of Status Epilepicus.
For example, carbamazepine can worsen epilepsy in children diagnosed with Dravet syndrome.
Cabanas ' daughter has Dravet syndrome and the family paid $ 300 a month for imported cannabis oil.
Sophie Gibson, six, suffers from severe form of epilepsy called Dravet syndrome.
Home > Rare epilepsies > Dravet syndrome.
Families and disability, managing parental stress for parents of children with Dravet syndrome.
IBE takes part in INDRE, new international research network in Dravet Syndrome and refractory epilepsy.
Charlotte Figi, for example is a little girl from Colorado who also suffers from Dravet syndrome.
This includes Parkinson 's disease and Dravet syndrome.
It all started with Charlotte Figi, a young girl suffering from the Dravet Syndrome.
CACNA1A variants may modify the epileptic phenotype of Dravet syndrome.
For patients 3 years of age or older with refractory SMEI or Dravet Syndrome.
Drug-resistant pediatric epilepsy, such as Dravet syndrome.
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