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What is another word for Infantile Severe Myoclonic Epilepsy?

Pronunciation: [ˈɪnfəntˌa͡ɪl sɪvˈi͡ə mˌa͡ɪəklˈɒnɪk ˈɛpɪlˌɛpsi] (IPA)

Infantile Severe Myoclonic Epilepsy, also known as Dravet Syndrome, is a rare and severe form of epilepsy that typically begins in infancy or early childhood. This condition is characterized by frequent seizures, often triggered by fever or illness, and accompanied by general developmental delays and cognitive impairment. Despite its lesser-known status, Dravet Syndrome has several synonyms that are used interchangeably in medical literature. Some of these include severe myoclonic epilepsy of infancy (SMEI), polymorphic epilepsy in infancy (PMEI), and recurrent polymorphic seizure disorder (RPSD). These terms reflect the varied and complex nature of the condition, emphasizing the severe myoclonic seizures that are the hallmark of Dravet Syndrome.
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What are the opposite words for Infantile Severe Myoclonic Epilepsy?

The antonyms for Infantile Severe Myoclonic Epilepsy (ISME) are health, stability, and normalcy. ISME is a rare form of epilepsy that affects infants and young children, causing severe seizures and developmental delay. The condition is marked by uncontrollable jerking movements, cognitive impairment, and other neurological symptoms that can greatly affect a child's wellbeing. However, with proper treatment and management, the symptoms of ISME can be controlled, allowing the affected individual to lead a healthy and fulfilled life. By contrast, antonyms of ISME, such as stability and normalcy indicate a life free of seizures and developmental delays, where individuals can pursue their goals and dreams with ease.

What are the antonyms for Infantile severe myoclonic epilepsy?

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