Convulsive Seizures
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Convulsion is an episode of abnormal violent and involuntary contraction of the muscle movements. Convulsion rarely last more than a few minutes and are extremely different in their manifestations. They occur when brain cells become too active and disorganized in their electrical properties. The characteristic of the seizures are determined by the site of origin of the abnormal brain discharge and the rapidity and extent to which the discharge spreads throughout the rest of the brain.
Causes of Convulsive seizures: Convulsive seizures occur in a variety of conditions and diseases involving the nervous system and other organs of the body. In some individuals who is experiences recurring seizures the exact nature of the underlying disease is not known, while in others, seizures have been associated with tumors, blood vessel abnormalities, disturbances in brain metabolism, brain scars, and other conditions. Traditionally, the term "epilepsy" is being use to describe the illness suffered by those with recurrent seizures.
Classification of Seizures:
- Grand Mal. Grand mal is one of the most common type of seizure, this type may occur at any age but they usually start before 25. During an attack there is a loss of consciousness, tongue biting, and urinary and fecal incontinence. There is also temporary cessation of breathing which causes bluish tinge of the skin followed by irregular snoring-like breathing. Gradually the patient relaxes, his breathing becomes normal, and he regains consciousness. Afterwards he may be confused, have headaches or gastric disturbances, or fall asleep. The attack may last from less than a minute to 10 minutes, but the post-seizure phrase may last for hours. Grand mal seizures may occur as often as several times a day or as infrequently as once every few years. Sometimes, they occur so close together that the patient does not regain consciousness between attacks.
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- Petit Mal. Petit Mal is a different kind of seizure (not a minor form of grand mal). Petit mal attacks usually occur in childhood and rarely persist after the age of 20. This attack is characterized by a sudden brief lapse of consciousness with or without minor movements of the eyes, head, or extremities, there may also be dropping of the head and on occasion, urinary incontinence. The attack lasts from 5 to 30 seconds after which the patient is alert and able to continue his normal activities. Despite their high frequency, attacks rarely occur.
- Psychomotor. Psychomotor seizure is characterized by a change in behavior and perception. Usually there is a clouding of the mind, total amnesia, and automatic movements during an attack. The movements are simple and brief, such as clamping the hands or smacking the lips, but they may also take the form of more complex behavior such as getting out of a chair and walking across a room. Aggressive behavior occasionally occurs, but rarely are violent acts committed. Attacks usually last 2 to 3 minutes and there may be a short of confusion afterward.
- Focal. When the attack is limited to one segment or function of the cerebrum, the term focal itself is applied, manifestations is directly related to the part of the brain involved. The convulsive movements usually begin in a finger and spread to the rest of the hand, the arm, the face, and the leg. If these movements spread to the opposite side of the body, the person loses consciousness and a grand mal attack may occur.
- Minor Motor. In minor motor the attack is brief, it occurs frequently, and lack post seizure abnormalities. This type usually occurs in childhood, but adults may sometimes experience them.
Three common types of minor motor seizure:
- akinetic seizures - is characterized by a sudden loss of muscle tone. The appearance depends on the muscles affected. "Head bobbing" occurs if the neck loses muscle tone, "bending seizures" occur if the upper extremities are affected, and "drop attacks" occur if the lower extremities are involved.
- myclonic seizures- are characterized by sudden brief involuntary contraction of the muscles of the trunk or extremities, it may occur singly or repetitively. One type of myoclonic seizure is infantile spasms, which usually occur at about 6 months of age and consist of sudden abduction of the upper extremity and flexion of the hip and knees. Myoclonic seizures may also occur in adolescents with gray matter disease and in adults with viral infections such as encephalitis.
- massive spasms - are characterized by strong contractions of most of the body's muscles, causing the patient to assume a "jackknife" position, with his arms flung upward, his head forward and down, and his lower limbs pulled up on the trunk. This position may last no longer than 5 to 10 seconds but may be repeated half a dozen times in a few minutes and innumerable times throughout the day.
Diagnosis. Diagnostic tests are essential in determining the exact type of seizure.
- Electroencephalogram is one of the most important tests to determine the type of seizure; it records the brain's electrical activities in the form of waves. It has been found that persons with grand mal, petit mal, and psychomotor seizures have characteristic brain waves.
- Pneumography injection of air into the brain spaces.
- Arteriography injection of dye into the arteries.
Treatment. The treatment of convulsive seizures consists of eliminating the causative factors (if they are known) and administering anticonvulsant drugs. Anticonvulsant drugs supresses the abnormal electrical activity of the brain regardless of the underlying cause. With appropriate treatment, most individuals suffering convulsions are able to lead normal and productive lives.
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Comments
excellent coverage of the topic of seizures. i may add that psychomotor seizures is also called complex partial seizures and is caused by temporal lobe disease and is also associated with Psychic symptoms, including visual and auditory hallucinations, a sense of unreality, and déjà vu.
thank you.
The delivery was by cesarean section, because to date revised 31 / 3 there were no signs, so we opted for surgery. Peter was very good. Cried and soon received a grade 9 scores. Was born with 48 cm and weighed 3.430 kilograms. Your first year of life was great, with perfect development and no disease. She sat with five months, walked at 11 months, said the first words at 7 months and before that already emit natural sounds of a baby. With a year and two months, one afternoon during sleep, Peter woke with a start as it was engasgando.Isso was repeated for a few more days until we went to the doctor. This saw a crisis, suspected of gastroesophageal reflux, and requested some tests.
At this time, these crises happened about 10 times a day and lasted about 15 seconds. As the tests did not show anything, on medical advice, seek a pediatric neurologist who said that it was seizures. We made a first electro encephalogram was normal. We seek Dr.Salomão Schwartzmam, which assessed and considered it logically perfect. During this period, seizures increased in number and intensity.
As of August 90 he was admitted to the ICU for the first time about one seizure every 3 minutes. It was in the hospital 20 days and left with the crisis more controlled. He made a CT scan that was normal. The second electro accused irritable focus on the right brain. Despite all this, its development was still normal, but showed to be more sleepy. The crisis continued, they were mixed seizures.
On October 90, realized that he was smiling less, less crying and when he smiled, the left side of his face was paralyzed. On November 90, realized that he wore at his left arm. Doctors called sequels. On December 90 we had a magnetic resonance imaging, a survey of eye examinations to detect some inborn errors of metabolism. All tests were normal.
At that time, he had difficulty walking and talking less. He kept an average of about 20 attacks per day. During seven months we changed doctors several times several anticonvulsants were tested. But the effect was never fully satisfatório.E was hospitalized two more times to manage crises more frequently. On January 91, Peter was admitted again and left the hospital without walking, sitting or falar.Em February, was hospitalized again with very strong attacks, spent 20 days in the hospital. The crisis has lasted for 1 min, manifesting itself every 10 min. At that time, was treated with cortisone and performed several tests of metabolism, but nothing was encontrado.A his motor skills was impaired. When was discharged, not holding his head, did not sit alone and did not seem to recognize anyone, and do not stare at nothing. Time passed, and with sections of physiotherapy and a lot of love Peter was getting some small progress.
We continued our marathon and medical examinations, but nothing happened. His seizures were a little more controlled, manifesting only during sleep, about 8 episodes per night, lasting about 1 min. At the end of 95, he was a few consecutive days without presenting crises.
In recent years, repeated some tests, but nothing new was encontrado.Teve pulmonary complications and took a lot of antibiotics. Over the past 95 months, Peter regained control of the head and gained more strength in the trunk. Spent to fix our gaze on people and objects, but not yet expressing a desire to get them. His face was more expressive, although not to laugh or cry.
On January 96, a repeat MRI showed that just like the previous one, according to the doctor who signed the report. Dr. Fernando Arita, your current doctor, who diagnosed Peter has a brain a little less dense than a child of 7 years.
Again also electro encephalogram, which presented much better than its predecessor, with more localized crises. We also made a study of karyotype (father, mother and son) with Dra.Rita of Cassia Stoco and nothing was found. He suspected Mitochondrial Diseases and suggested that we make a study of DNA. There was also a dose of amino acids in the blood and
chromatography of sugars in urine.
Currently, Peter has about 4 seizures during sleep, mostly from the morning. In its crises stretching arms and legs, turns his head to the left and cries. They last about 45 seconds. His attention remains fixed on people and objects, but does not move spontaneously. It recovered its reasonable control of the trunk, but do not sit, not stand, do not talk, does not smile or cry.
Two years has developed a scoliosis very worrying. Are treated with Rivotril, Valpakine and Tryleptal.
Peter currently is 15 years. During all these years, did not find an answer to what happens to Peter, and also never find someone with similar problem to share experiences.
If you can help, if medical or ever met a child with the same problem, please write to us. Thank you very much. Liane and Manoel.
Rua Conselheiro Brotero, 1559 apto 134 - CEP 01232-011 São Paulo - Phone: (11) 3662.4826











jopeppi says:
4 months ago
thanks for the info