Author Archives: eCreative Studios

Startle Epilepsy

August 8, 2011

Startle epilepsy is a type of reflex epilepsy in which seizures are provoked by loud noises or sudden surprises. Most patients with startle epilepsy are only sensitive to one sensory modality (i.e. temperature, taste, sound, pressure). However, it is the unexpected nature of the stimulus rather than the sensory modality that characterizes startle epilepsy.

Patients with startle epilepsy usually have static cerebral lesions and developmental delay. Many of the patients are hemiparetic, meaning half of the body is partially paralyzed, and it is the weak side of the body that is primarily involved in the startle seizures. Startle epilepsy is often associated with disorders such as infantile hemiplegia, Down syndrome, anoxic encephalopathy, and cortical dysplastic lesions.

These seizures usually last less than 30 seconds. The seizure begins with a startle response, followed by a brief tonic phase. Patients sometimes fall to the ground and experience clonic jerks. Responsiveness to the stimulus decreases as a result of repeated exposure to the stimulus. Spontaneous seizures also occur in patients with startle epilepsy, but are infrequent in most cases.

Carbamazepine, clonazepam, clobazam, and lamotrigine are sometimes prescribed for patients with startle epilepsy. Surgery has been reported to control startle epilepsy associated with infantile hemiplegia, but startle epilepsy is typically intractable. Patients can usually only achieve incomplete or temporary seizure control.

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Simple Partial Seizures

August 8, 2011

(Focal Cortical Seizures)

Simple partial seizures result from epileptic activity localized in one part of the brain, usually the cortex or limbic system.

Consciousness is not impaired. Someone experiencing a simple partial seizure can talk and answer questions. S/he will remember what happened during the seizure.

Simple partial seizures take different forms in different people. They are further classified according to their symptoms:

  • Autonomic Seizures – These seizures are accompanied by autonomic symptoms or signs, such as abdominal discomfort or nausea, which may rise into the throat (epigastric rising), cause stomach pain, the rumbling sounds of gas moving in the intestines (borborygmi), belching, flatulence and vomiting. This has sometimes been referred to as abdominal epilepsy. Other symptoms may include pallor, flushing, sweating, hair standing on end (piloerection), dilation of the pupils, alterations in heart rate and respiration, and urination. A few people may experience sexual arousal, penile erection, and orgasm.
  • Emotional and Other – Simple partial seizures, which arise in or near the temporal lobes, often take the form of an odd experience. One may see or hear things that are not there. One feels emotions, often fear, but sometimes sadness, anger, or joy. There may be a bad smell or a bad taste, a funny feeling in the pit of the stomach or a choking sensation. These seizures are sometimes called simple partial seizures of temporal lobe origin or temporal lobe auras.
  • Motor – Other simple partial seizures include (clonic, jerking) convulsive movements. Jerking typically begins in one area of the body — the face, arm, leg, or trunk — and may spread to other parts of the body. These seizures are sometimes called Jacksonian motor seizures while their spread is called a Jacksonian march. It cannot be stopped.
  • Sensory Seizures – Some simple partial seizures consist of a sensory experience. The person may see lights, hear a buzzing sound, or feel tingling or numbness in a part of the body. These seizures are sometimes called Jacksonian sensory seizures.

Simple partial seizures usually last just a few seconds, although they may be longer. If there are no convulsions, they may not be obvious to the onlooker.

In some children, simple partial seizures lead to complex partial seizures, or to tonic-clonic convulsions.

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Secondarily Generalized Seizures

August 8, 2011

Secondarily generalized seizures are usually partial seizures evolving into generalized seizures, most often with tonic-clonic convulsions. The partial seizures, which were once limited to one hemisphere of the brain, progress to encompass the entire brain bilaterally. This causes a generalized seizure. The clinical nature of a secondarily generalized seizure usually does not differ from that of the initial, originating seizure.

Secondarily generalized seizures are predominant in 16 per cent of all children and 9 per cent of all adults with seizure disorders. Most people with complex partial seizures and many with simple partial seizures will experience a secondarily generalized seizure at some point. When they occur frequently, the chances for future partial seizures may be increased.

Secondarily generalized seizures occur infrequently and are easily controlled by anti-epileptic medication.

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Rolandic Epilepsy

August 8, 2011

(Sylvan Seizures)

Benign rolandic epilepsy is so named because the focus of repetitive spike activity in the brain is predominantly within the mid-temporal or parietal areas, near the motor or rolandic strip.

Seizures usually occur infrequently as generalized nocturnal seizures characterized by a variety of minor tonic-clonic movements, often affecting only one side of the face. A seizure begins with a sensation starting at the corner of the mouth, followed by jerking of that corner. The jerking may then spread to the rest of that side of the face, in turn causing a twisting motion.

Excessive salivation occurs, along with possible speech arrest. The child usually does not lose consciousness, except in cases of secondarily generalized seizures of this type. In rare cases, the seizure may progress to encompass the entire side of the body, becoming a generalized tonic-clonic condition.

Onset is usually after three years of age. One quarter of school-age children with epilepsy may have rolandic seizures. The condition is benign and is frequently outgrown by adolescence.

Medication is not prescribed generally. In chronic cases, carbamazepine or phenytoin may be prescribed. It is tapered off and discontinued after puberty or after a seizure-free period of three years.

Click here to learn about other types of seizures.