Haan J, Terwindt G M, Ferrari M D
Department of Neurology, Leiden University Hospital, The Netherlands.
Neurol Clin. 1997 Feb;15(1):43-60. doi: 10.1016/s0733-8619(05)70294-2.
Although family studies and twin studies are not sufficiently reliable to establish this theory with certainty, migraine likely is influenced by hereditary susceptibility. The association of migraine with a large number of hereditary diseases opens the possibility to choose candidate chromosomes for linkage studies. A rare subtype of migraine, familial hemiplegic migraine, is linked to chromosome 19p and at least one other locus. The chromosome 19p also seems to be involved in "normal" migraine, although conflicting results have been reported.
尽管家族研究和双生子研究不足以可靠地确定这一理论,但偏头痛很可能受到遗传易感性的影响。偏头痛与大量遗传性疾病的关联为连锁研究选择候选染色体提供了可能性。偏头痛的一种罕见亚型,家族性偏瘫性偏头痛,与19号染色体短臂及至少一个其他位点相关联。19号染色体短臂似乎也与“普通”偏头痛有关,尽管已有相互矛盾的报道。