Dravet syndrome or severe myoclonic epilepsy of infancy (SMEI) is a progressive encephalopathy associated with difficult-to-control seizures and, often, profound intellectual disability, representing one of the greatest risks of sudden and unexpected death in children. patients with epilepsy.
<h3>What are the signs and symptoms of a Dravet syndrome?</h3>
Seizure Symptoms include involuntary body movements, blue lips, loss of consciousness, excessive saliva and upturned eyes. The moment of crisis can be frightening for some, but it is essential to remain calm and try to help the patient.
<h3>Dravet Syndrome Diagnosis</h3>
Early diagnosis is critical, combining clinical diagnosis with a genetic diagnosis. However, the clinical diagnosis can prove to be difficult, because in many patients with the syndrome all signs are not observed. Therefore, in case of clinical suspicion of DS, it is essential to resort to genetic diagnosis, which can identify SCN1A alteration, confirming the diagnosis.
With this information, we can conclude that Dravet Syndrome (DS) is a rare, progressive and disabling genetic disorder, also known as severe myoclonic epilepsy of childhood.
Learn more about Dravet Syndrome in brainly.com/question/9782041
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