myoclonia$51303$ - vertaling naar italiaans
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myoclonia$51303$ - vertaling naar italiaans

SEVERE EPILEPSY SYNDROME WITH INFANTILE SPASMS, HYPSARRHYTHMIA AND MENTAL RETARDATION
Jackknife convulsion; Salaam spasm; Infantile epileptic encephalopathy; Generalized flexion epilepsy; Infantile myoclonic encephalopathy; Infantile spasm; Massive myoclonia; Spasms, infantile; West's syndrome; West Syndrome; Juvenile spasm; Infantile spasms; West syndrome; Salaam spasms

myoclonia      
n. mioclonia (medicina- contrazioni muscolari brusche, involontarie che si ripetono ad intervalli variabili)

Wikipedia

Epileptic spasms

Epileptic spasms is an uncommon-to-rare epileptic disorder in infants, children and adults. One of the other names of the disorder, West syndrome, is in memory of the English physician, William James West (1793–1848), who first described it in an article published in The Lancet in 1841. The original case actually described his own son, James Edwin West (1840–1860). Other names for it are "generalized flexion epilepsy", "infantile epileptic encephalopathy", "infantile myoclonic encephalopathy", "jackknife convulsions", "massive myoclonia" and "Salaam spasms". The term "infantile spasms" can be used to describe the specific seizure manifestation in the syndrome, but is also used as a synonym for the syndrome itself. West syndrome in modern usage is the triad of infantile spasms, a pathognomonic EEG pattern (called hypsarrhythmia), and developmental regression – although the international definition requires only two out of these three elements.

The syndrome is age-related, generally occurring between the third and the twelfth month, generally manifesting around the fifth month. There are various causes. The syndrome is often caused by an organic brain dysfunction whose origins may be prenatal, perinatal (caused during birth) or postnatal.