Giordano L, Accorsi P, Valseriati D, Tiberti A, Menegati E, Zara F, Vignoli A, Vigevano F
Department of Child and Adolescent Neuropsychiatry, Spedali Civili, Brescia, Italy.
Neuropediatrics. 1999 Apr;30(2):99-101. doi: 10.1055/s-2007-973469.
We present a patient (3 months old) with partial and generalized seizures who has a family history of seizures with a onset during the first 12 months of life. We diagnosed benign infantile familial convulsions (BIFC) and we did not introduce any antiepileptic therapy. We present clinical data of her family where 18 out of 35 members were affected; to our knowledge this is the largest family with BIFC. BIFC is transmitted as an autosomal dominant trait; recently it has been reported that the gene for BIFC maps to the long arm of chromosome 19. We conducted linkage analysis in our family providing significant exclusion of linkage between the BIFC locus phenotype and chromosome 19 markers, suggesting that a second locus is involved in this family.
我们报告了一名3个月大的部分性和全身性癫痫患儿,其家族中有在出生后12个月内发病的癫痫病史。我们诊断为良性婴儿家族性惊厥(BIFC),未采用任何抗癫痫治疗。我们展示了其家族的临床数据,35名家族成员中有18人患病;据我们所知,这是最大的BIFC家族。BIFC以常染色体显性性状遗传;最近有报道称,BIFC基因定位于19号染色体长臂。我们对该家族进行了连锁分析,结果显示BIFC位点表型与19号染色体标记之间不存在连锁关系,提示该家族存在第二个相关位点。