
Myoclonic-atonic seizures (EMAS) are a rare type of epilepsy that affects children. Seizures are triggered by aberrant electrical firings in the brain. Epilepsy is characterised by recurrent seizures.
Previously known as Doose syndrome, epilepsy with myoclonic atonic seizures is a syndrome marked by the typically sudden development of several generalized seizure types, including myoclonic-atonic seizures in early childhood. The period of active seizures is usually when developmental standstill or regression occurs. Two-thirds of children who have epilepsy attain remission despite having seizures that are initially resistant to medication.
In EMAS, the initial seizure often happens between the ages of two and six.
The first seizure happens during a fever in 1 in 4 children. EMAS is more common in boys than in girls. The majority of seizures in children with EMAS are generalized seizures, or seizures that impact the entire brain. Focal seizures are uncommon in EMAS and only impact one area of the brain. Multiple seizure types can be included in EMAS, including:
Seizures in EMAS can occasionally alter a child's state of consciousness. This may occur in the absence of overt seizure symptoms. For example, there might not be any jerking. This is known as nonconvulsive status epilepticus when it happens and persists for a long time.
Seizures that are myoclonic-atonic are the main sign of EMAS. However, developmental setbacks might also be a sign. As EMAS develops, they are observed. A child's development is often normal or just slightly delayed when seizures start. Around the same time as the seizures start, developmental impairments start. Although there may be another cause for both, many researchers think that the seizures are a contributing factor to the developmental deficits. Children with EMAS may have parents who report:
Causes
Risk Factors
In addition to seizures, people with epilepsy may also have other health issues. The epilepsy itself may cause these issues, or they may be related to the seizures. For instance, they might have mood swings, adjustments to the timing of seizures, or adverse drug reactions. Others could have trouble sleeping, thinking and remembering things, or interacting with people. Rarely, SUDEP (Sudden Unexpected Death in Epilepsy) or early death may transpire.
Complications
EMAS complications are that, rarely, people with epilepsy may pass away unexpectedly. While some people may have seizures that are simple to manage, others may have more severe seizures that may require emergency care.
Myoclonic-atonic epilepsy (MAE) is usually treated in Malaysia with first-line drugs. The ketogenic diet has demonstrated efficacy in lowering seizure frequency in patients who are resistant to treatment. For refractory instances, vagus nerve stimulation (VNS) is also being investigated. Genetic testing is increasingly being employed to tailor treatment regimens for improved results.
Vagus Nerve Stimulation: By delivering frequent, mild electrical energy pulses to the brain through the vagus nerve, vagus nerve stimulation (VNS) can either prevent or reduce seizures. A device is implanted beneath the skin in the left chest region as part of the therapy. The generating device is connected to an electrode or wire that is positioned beneath the skin. The vagus nerve in the neck is where the wire is fastened or coiled. The gadget is configured to administer stimulation or pulses at predetermined intervals in the outpatient clinic. This device operates without the user having to do anything. When a VNS device is operating, the user is typically unaware of the stimulation. A person can transmit an additional burst of stimulation to the brain by swiping a magnet over the generator in the left chest area if they are aware of when a seizure occurs. This may help prevent seizures for some people.
Cost Start From USD 15000 - USD 25000Explore Options
When myoclonic-atonic seizures are observed by family members or medical professionals, EMAS is diagnosed. A physical examination and medical history might give doctors some information regarding the seizures. They might inquire about the types of seizures and the onset of seizures. To find out more, they frequently employ laboratory studies.
Additional indicators of an EMAS diagnosis include:
MediRehab (a chain of Rehab centres, part of MediGence) provides comprehensive rehabilitation services to support patients through Teleconsulations and online therapy sessions.
Children with MAE who experience prolonged or frequent seizures may require rescue therapy or emergency medical attention. Diazepam rectal gel (Diastat) or another benzodiazepine administered under the tongue or intranasally into the nose are examples of rescue therapy.
For information on seizure crises and choices for home rescue medication, parents of children with MAE should speak with their treating neurologist or other healthcare professional.
Children may require immediate medical attention if rescue medication fails to halt seizures or if they are suspected of having non-convulsive status epilepticus, which is characterized by reduced consciousness, drooling, unsteadiness, and twitching of the arms, legs, or face.
Depending on the situation, your healthcare professional may prescribe medicine to help control your symptoms and support the treatment plan.









Kuala Lumpur, Malaysia
Sunway Medical Centre has initiated a comprehensive expansion plan close to its current hospital facility to enhance its ability to provide services to the global market. The new Cancer Radiosurgery Center and Nuclear Medicine Center, which will also house additional Centers of Excellence like the Digestive Health Center and Dialysis Center, marked the completion of Tower C's first phase in October 2016.

Kuala Lumpur, Malaysia
Situated at the junction of Petaling Jaya and Shah Alam, close to the Oasis Ara, Ara Damansara Medical Centre boasts a serene, luxurious ambiance.
The Centre has been awarded several prestigious awards such as the Global Health Asia Pacific Awards 2023, Newsweek Best Specialized Hospital APAC 2023, Healthcare Asia Awards 2023, and Malaysian Healthcare Wellness Excellence.

Kuala Lumpur, Malaysia
Prince Court is a private medical facility in the center of Kuala Lumpur that has 277 individual beds. Our dedication is to provide you with the best treatment possible from the time you arrive until you depart, healthier and happier. We are well-known for our top-notch facilities, cutting-edge technology, and friendly customer service.
Opinion & Option
We submit the most accurate opinion and options from one or more countries for your review
Consult Privately
Consult with a certified specialist privately on our telemedicine platform even before you decide to travel
Logistics
We handle flights, visas, transfers, and accommodation—so you can focus on your health.
Recovery
Our In-house rehabilitation service packages to better your recovery and treatment outcome
There are several reasons to select Malaysia for Myoclonic Atonic Epilepsy Treatment:
Although there is no known cure for myoclonic atonic seizures, some people can completely control them with medication and vagal nerve stimulation therapy. Epilepsy surgery can occasionally stop myoclonic seizures in some patients who have myoclonus due to focal epilepsy. However, once myoclonic seizures have started, it is impossible to tell if a person will outgrow them. Some patients with myoclonic atonic epilepsy have seizures that are resistant to medication, making treatment challenging. Managing seizures and reducing the risk of developmental delays requires early treatment with the right medicine and close observation.
Myoclonic Atonic Epilepsy (MAE) can be effectively treated in Malaysia through advanced drugs that drastically lower seizure frequency. Long-term patient outcomes are improved with individualised treatment provided by multidisciplinary care.
Yes, contemporary diagnostic methods like EEG and neuroimaging, as well as cutting-edge therapies like deep brain stimulation and customised drug regimens, are available in Malaysian hospitals for the treatment of myoclonic atonic epilepsy. These technologies aid in providing patients with accurate and efficient care.
Always consider the following factors when selecting Malaysian hospitals:
In Malaysia, treatment for myoclonic atonic epilepsy has a promising success rate; many patients report a reduction in seizure frequency of more than 50%. Patients' quality of life and overall results are enhanced by multidisciplinary care.
A single test cannot diagnose EMAS. Instead, Myoclonic Atonic Epilepsy must be diagnosed by physicians using clinical data, laboratory testing, and tests like electroencephalograms.
This kind of epilepsy is extremely severe and becomes worse over time. It typically involves brain damage or degradation that impacts memory, motor control, cognitive function, and other areas. In some cases, this can lead to death.
The "cure" for Myoclonic Atonic Epilepsy (MAE) cannot be performed before birth.
Although some parents purchase off-the-shelf solutions, such as hockey helmets, a neurologist or hospital can supply a safe helmet for your child. Injury prevention at home can be achieved by installing baby gates and erecting safety barriers around fireplaces and furniture. Specialised dining utensils and safety mats provide even more protection during regular tasks.
Yes, you can consult a Malaysian expert for a second opinion. Prominent medical facilities and knowledgeable physicians provide consultations to go over diagnoses and suggest the best course of action. You can get support by speaking with a medical tourism facilitator at MediGence to select the best doctor and facility. It provides specialised rehabilitation programs.