该病属常染色体隐性遗传，与X-染色体关联，所以，母亲是基因携带者的男性表现为发病。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
因为布林先生最近发现，他从母亲那里遗传了一个变异的基因LRRK2。 研究显示，变异的LRRK2可能使得有家族患病史的携带者患帕金森氏症的几率增加。
The reason was that Mr Brin had recently discovered that he has inherited from his mother a mutation of a gene called LRRK2 that appears to predispose carriers to familial Parkinson’s.
通过遗传咨询门诊，对反复性流产患者夫妇双方或一方进行了染色体核型分析，共71例，检出平衡易位携带者3例。
The karyotypes cf 71 cases of recurrent abortion, or their couples were examined in genetic definition clinic, 3 cases of anomalous karyotype were observed.
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