Skre H, Berg K
Clin Genet. 1977 Jan;11(1):57-66. doi: 10.1111/j.1399-0004.1977.tb01279.x.
Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism were observed in two kindreds, and they were found to occur togetherin 9 out of 10 affected individuals. The last patient had Marinesco-Sjøgren syndrome without manifestations of hypogonadism, and similar findings were observed in two affected sisters from a third kindred. On the hypothesis that the concurrence of Marinesco-Sjøgren syndrome and hypergonadotropic hypogonadism was caused by linkage, a lod score analysis was conducted. Four sibships in the two kindreds were informative with respect to linkage. At the recombination fraction 0.05, the lod score exceeded 3. If linkage causes the concurrence of Marinesco-Sjøgren syndrome and hypergonadotropic hypongonadism in these kindreds, the linkage is close. No linkage was observed between the clinical syndromes and 17 marker systems.
在两个家族中观察到马里内斯科-舍格伦综合征和高促性腺激素性性腺功能减退,并且在10名受影响个体中有9名发现这两种疾病同时出现。最后一名患者患有马里内斯科-舍格伦综合征但无性腺功能减退表现,在来自第三个家族的两名受影响姐妹中也观察到类似结果。基于马里内斯科-舍格伦综合征和高促性腺激素性性腺功能减退同时出现是由连锁引起的这一假设,进行了对数优势计分分析。两个家族中的四个同胞对连锁具有信息价值。在重组率为0.05时,对数优势计分超过3。如果连锁导致这些家族中马里内斯科-舍格伦综合征和高促性腺激素性性腺功能减退同时出现,那么这种连锁关系紧密。在临床综合征与17个标记系统之间未观察到连锁关系。