Carton D
Neuropadiatrie. 1978 May;9(2):167-71. doi: 10.1055/s-0028-1085421.
A male neonate presented with very frequent seizures, from the second day of life until the age of two weeks. Subsequently, convulsions did not recur. The patient, 7 years of age at present, has developed normally. Family history revealed transient neonatal convulsions in 8 other family members. The condition is inherited as an autosomal dominant trait.
一名男婴自出生第二天起直至两周大时出现频繁癫痫发作。随后,惊厥未再复发。该患者目前7岁,发育正常。家族史显示其他8名家庭成员有短暂性新生儿惊厥。该病以常染色体显性性状遗传。