Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Type of study
Language
Year range
1.
JBM-Journal de Biologie Medical. 2018; 7 (25): 26-29
in French | IMEMR | ID: emr-203852
2.
Maroc Medical. 2006; 28 (1): 13-16
in French | IMEMR | ID: emr-78980

ABSTRACT

Landau-Kleffner syndrome is a rare disorder caraterised by acquired aphasia of children, paroxysmal electroencephalographic disturbance and in 75% of cases epileptic seizures and cognitives disturbances. We report a 6 year old daughter who presented epileptic seizures and six months later regression langage and a behaviour of deaf. This patient had a global aphasia. The understanding was affected because of the cortical deafness. The electroencephalogramme showed discharges in the temporal bilateral regions. The cerebral scan and the potential evoked auditory were normal. The Landau-Kleffner syndrome's diagnosis was confirmed. The patient was treated by valproic acid and corticosteroids with good evolution. The stoopage of treatment has brought more seizure and the worsening aphasia. The authors discussed the pathogenic hypothesis, the semiology and the treatment of the Landau-Kleffner syndrome


Subject(s)
Humans , Female , Aphasia , Epilepsy , Landau-Kleffner Syndrome/drug therapy , Valproic Acid , Adrenal Cortex Hormones
SELECTION OF CITATIONS
SEARCH DETAIL