Case of Infantile Convulsions
نویسنده
چکیده
منابع مشابه
Effects of Infantile Repeated Hyperglycemia on Neuronal Density of Hippocampus and Pentylentetrazol Induced Convulsions in Male Wistar Rats
Objective(s) High blood glucose induces molecular, cellular, morphological and behavioral changes in the brain. Metabolic disturbances, contribute to the hippocampus injury and development of partial focal seizures. The aim of this study was to investigate the effects of infantile repeated hyperglycemia on neuronal density of hippocampal CA3region in newborn Wistar male rats and its effect on ...
متن کاملThe PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions
PURPOSE Mutations in the PRRT2 gene have been recently described as a cause of paroxysmal kinesigenic dyskinesia, infantile convulsions with choreoathetosis syndrome and, less often, infantile convulsions. We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia. METHODS AND RESULTS Direct sequencing of ...
متن کاملگزارش یک مورد اسپاسم شیرخوارگی در زمینه تو بروس اسکلروزیس
ABSTRACT Tuberous Sclerosis(T.S) is an inherited disease (with autosomal dominant trait). It is characterised by different skin manifestations involvement of central nervous system and hamartomas in different organs of the body .Of Course ,about 10% of cases are due to new mutations Presentation of this patient, a 4-month-old male infant with recurrent convulsions cflexor type infantile spasm ...
متن کاملBrain dysfunction in infantile febrile convulsions.
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متن کاملGenetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.
PURPOSE PRRT2 mutations were recently identified in benign familial infantile epilepsy (BFIE) and infantile convulsions with paroxysmal choreoathetosis (ICCA) but no abnormalities have so far been identified in their phenotypically similar seizure disorder of benign convulsions with mild gastroenteritis (CwG), while mutations in KCNQ2 and KCNQ3 have been recognized in benign familial neonatal e...
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عنوان ژورنال:
دوره 3 شماره
صفحات -
تاریخ انتشار 2017