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L Marques-Assis

Publications and source records attributed to L Marques-Assis.

13 recordsLinked to original sources

Mental deterioration in Lafora's disease.

Lafora's disease is included among the progressive myoclonic epilepsies. Despite the fact that dementia is a constant finding in this disease only a few papers have studied the timing of mental deterioration. We have performed wide neuropsychological testing in two cases early diagnosed as Lafora disease. The initial neuropsychological testing was carried out by the time there were no complaints of mental deterioration in both cases. In the first case consecutive neuropsychological testing demonstrated the rapidly progressive dementia. All neuropsychological testings in these cases showed severe impairment of right parietal lobe functions. Higher cortical functions related to language and intellectual processes were best preserved in both cases. The functions related to constructional praxis, memory and abstract concepts and processes were severely impaired. Our data suggest that mental deterioration is an early manifestation in Lafora disease, even by the time normal social life is not yet disturbed. Dominant hemisphere cognitive functions have been less impaired than the non-dominant ones. How a diffuse illness such as Lafora disease can cause such an asymmetrical higher cortical function deficit is not yet clear.

Adolescent

[Primary reading epilepsy: therapeutic efficacy of clonazepam in one case].

Primary reading epilepsy is a rare form of reflex epilepsy, in which reading is the specific stimulus evoking attacks. The authors report a case of an 18-year-old man who since the age of 17 presented myoclonic jaw jerking provoked exclusively by reading. In one episode, in which reading was not interrupted, jerks were followed by a generalized convulsive seizure. EEG with routine activating procedures was normal, while EEG recorded during reading showed bilaterally synchronous paroxysmal small-voltage spikes, more prominent in frontocentral regions, coinciding with jaw myoclonus. Complete clinical seizures control and EEG normalization were achieved with clonazepam 2 mg daily in a 24-month follow-up.

Adolescent

[Suppression of drug therapy in epilepsies].

A group of 36 epileptic patients is studied; in 35 the drug was suppressed and in 1 the treatment was not started. The group was compared with epilepsy in general regarding to the age of onset, the time of the disease, the frequency of the seizures, the clinical manifestations and the EEG pattern. In view of the results attained by the investigation the author draws the following conclusions: 1) in the group studied the onset of the disease prevailed at the second decade of life; 2) the disease duration was lower than 1 year in 55% of the cases; 3) the cases submitted to early treatment predominate in the group studied; 4) the patients with pure convulsive seizures predominate when compared to those with focal convulsive fits; significant differences were not found when the EEG pattern of the group studied was compared with epilepsy in general; the rate of normal EEG was similar in both groups.

Anticonvulsants

[Epilepsy and work].

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Adolescent