Benign familial neonatal convulsions.
نویسندگان
چکیده
Benign familial neonatal convulsions are a rare genetic seizure disorder inherited as an autosomal dominant trait. They consist of brief episodes of seizures, recurring during the first few days or weeks of life in otherwise normal babies; their prognosis is good. We report a family in which at least 12 members in three generations presented with this condition; they all had an excellent outcome.
منابع مشابه
Benign familial neonatal convulsions: abnormal intrauterine movements, provocation by feeding and ICTAL EEG
An infant with benign familial neonatal convulsions had abnormal movements during the last 2 months of pregnancy suggestive of intrauterine seizures. His postnatal seizures, one of which was captured by electroencephalography, had both partial and generalized features. Most seizures appeared to be provoked by feeding.
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Benign familial neonatal convulsion is a rare autosomal dominant inherited epilepsy syndrome characterized by unprovoked seizures in the first few days of life, normal psychomotor development, and a positive intergenerational family history of neonatal seizures. Over 90% of the affected individuals have inherited causal mutations in KCNQ2, which encodes for the potassium voltage-gated channel s...
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Neonatal seizures represent a heterogeneous group of disorders with vastly different etiologies and outcomes. Benign familial neonatal convulsions (BFNC) are a distinctive epileptic syndrome of autosomal dominant inheritance with a favorable prognosis, characterized by the occurrence of unprovoked partial or generalized clonic seizures in the neonatal period or early infancy. Recently, mutation...
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ورودعنوان ژورنال:
- The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
دوره 9 3 شماره
صفحات -
تاریخ انتشار 1982