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Dravet Syndrome Treatment

Dravet Syndrome

Dravet syndrome is a rare and severe form of epilepsy that typically begins in infancy. Here’s a brief overview of its symptoms, causes:


  1. Seizures: Dravet syndrome is characterized by recurrent seizures, often starting within the first year of life. These seizures can be prolonged and may involve multiple seizure types, including tonic-clonic, myoclonic, and absence seizures.
  2. Developmental Delays: Children with Dravet syndrome often experience developmental delays, including delays in speech and motor skills.
  3. Behavioral and Cognitive Issues: Some children with Dravet syndrome may exhibit behavioral and cognitive issues, such as hyperactivity, aggression, and difficulty with social interactions.
  4. Temperature Sensitivity: Seizures in Dravet syndrome are often triggered by fevers, hot temperatures, or warm baths.

Causes: Dravet syndrome is primarily caused by genetic mutations, most commonly in the SCN1A gene. This gene provides instructions for making a protein involved in the function of sodium channels in the brain. Mutations in this gene disrupt the normal function of sodium channels, leading to abnormal electrical activity in the brain, which can trigger seizures.

Homeopathy Treatment

Dravet syndrome, also known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare and severe form of epilepsy that begins in infancy. It’s characterized by frequent seizures, developmental delays, and other neurological issues.

Homeopathy, a form of alternative medicine, operates on the principle of “like cures like,” where a substance that causes symptoms in a healthy person is used to treat similar symptoms in a sick person. While some individuals may seek homeopathic treatment for Dravet syndrome, it’s important to note that there’s limited scientific evidence supporting its efficacy in managing this condition.

Homeopathic treatments for Dravet syndrome may vary depending on the individual’s symptoms and constitution. Remedies commonly used in homeopathy for epilepsy-related symptoms might include Cuprum metallicum, Cicuta virosa, or Bufo rana, among others. However, it’s crucial for anyone considering homeopathic treatment for Dravet syndrome to consult with a qualified healthcare professional, ideally one who is knowledgeable about both conventional and alternative medicine approaches. They can provide guidance on the appropriateness and safety of such treatments, as well as ensure that they complement any conventional treatments the individual may be receiving.

Naturopathy Treatment

Naturopathy focuses on supporting the body’s natural ability to heal and maintain itself. Some naturopathic approaches that may be beneficial for individuals with Dravet syndrome include:

  1. Nutritional Support: A naturopathic approach often emphasizes a nutrient-rich diet that supports overall health and neurological function. This might include whole foods rich in antioxidants, vitamins, and minerals. Some individuals may benefit from specific dietary interventions, such as a ketogenic diet, which has shown promise in reducing seizures in some epilepsy patients.

  2. Herbal Medicine: Certain herbs may have anticonvulsant properties or help manage symptoms associated with Dravet syndrome. However, it’s crucial to use caution and consult with a qualified naturopath or healthcare provider, as herbs can interact with medications or exacerbate certain health conditions.

  3. Lifestyle Modifications: Naturopathy often emphasizes lifestyle factors such as stress management, adequate sleep, regular exercise, and minimizing exposure to environmental toxins. These factors can influence overall health and may help improve seizure control and quality of life.


For Dravet Syndrome Treatment

Dravet syndrome is a rare and severe form of epilepsy that typically begins in infancy. It is characterized by frequent and prolonged seizures, developmental delays, and other neurological issues.

Dravet syndrome is typically caused by a genetic mutation in the SCN1A gene. This gene provides instructions for making a sodium channel that plays a crucial role in the normal function of brain cells. Mutations in this gene can disrupt the balance of sodium ions in brain cells, leading to seizures and other symptoms of Dravet syndrome.

Currently, there is no cure for Dravet syndrome. Treatment focuses on managing symptoms, reducing seizures, and improving quality of life through a combination of antiseizure medications, dietary therapies, supportive therapies, and other interventions.

Treatment for Dravet syndrome often involves a combination of approaches, including antiseizure medications, dietary therapies (such as the ketogenic diet), vagus nerve stimulation (VNS), CBD-based medications, and supportive therapies (such as physical therapy and occupational therapy).

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