Characteristics of infantile spasms
Infantile spasms is a unique, and frequently malignant, epileptic confined to infants. This syndrome has three characteristic features:15,16
Age of onset
Infantile spasms are an age-specific disorder beginning in children during the first 2 years of life. It is unusual for infantile spasms to begin after 18 months, however. Most infantile spasms begin before 12 months of age, clustering between 4 and 7 months.
Types of spasms
Some seizures are characterized by brief head nods, whereas others consist of violent flexion of the trunk, arms, and legs. Infantile spasms can be classified into three major groups:17
Asymmetric spasms also occasionally occur. These consist of maintenance of a “fencing” posture.
Most patients have more than one seizure type.
Frequency of spasms
Infantile spasms frequently occur in clusters, and the intensity and frequency of the spasms in each cluster may increase to a peak before progressively decreasing. The seizures are very brief, so casual observers may miss single seizures. The number of seizures per cluster varies considerably, with some clusters consisting of as many as 150 seizures. The number of clusters per day also varies, with some patients having as many as 60 clusters per day.
Clusters occur rarely during sleep but frequently are seen shortly after awakening. Crying or irritability during or after a flurry of spasms is commonly observed. The number of infantile spasms occurring at night is similar to the number occurring during the day.
Infantile spasms are associated with markedly abnormal EEGs. The most commonly found EEG pattern is ,18 which consists of a high-voltage, slow record dominated by delta activity with frequent and multifocal spikes, sharp waves, and and slow wave complexes(Figure 1). Variations of hypsarrhythmia include:18
During sleep, especially rapid-eye-movement (REM) sleep, a marked reduction or total disappearance of the hypsarrhythmic pattern may be noted. Although the hypsarrhythmic or modified hypsarrhythmic pattern is the most common type of abnormality seen in infantile spasms, it is not seen in all patients who have this disorder.
Adapted from: Holmes GL. Childhood-specific epilepsies accompanied by developmental disabilities: Causes and effects. In: Devinsky O and Westbrook LE, eds. Epilepsy and Developmental Disabilities. Boston: Butterworth-Heinemann; 2001;23–32.
Reviewed and revised May 2004 by Steven C. Schachter, MD, epilepsy.com Editorial Board.
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