Percy M E, Markovic V D, Crapper McLachlan D R, Berg J M, Hummel J T, Laing M E, Dearie T G, Andrews D F
Neurogenetic Laboratory, Surrey Place Centre, Toronto, Ontario Canada.
Am J Med Genet. 1991 Jun 1;39(3):307-13. doi: 10.1002/ajmg.1320390312.
We have identified 2 sisters with probable dementia of the Alzheimer type who have an unusual 22-derived marker chromosome with a greatly elongated short arm containing 2 well-separated nucleolus organizer regions. A marker chromosome similar in appearance is uncommon in the general population. Eleven of 24 of their biological relatives were also found to have the marker. The known pedigree of this family encompasses 6 generations in 2 of which there is evidence of 10 cases of dementia of the Alzheimer type. The average age-at-onset of dementia is 65.8 +/- 5.5 years; the average age-at-death among those apparently affected is 74.9 +/- 8.3 years. A new model for the estimation of risk was applied to the family data. Persons in this family with the marker were found to be 4 times more likely to develop dementia than those without the marker, the 95% confidence interval for this risk being 1-50. The probability that the association of dementia and the marker is due to chance alone is .05 (1 in 20).
我们发现了2名患有可能的阿尔茨海默型痴呆症的姐妹,她们有一条异常的源自22号染色体的标记染色体,其短臂大大延长,包含2个分隔良好的核仁组织区。外观相似的标记染色体在普通人群中并不常见。她们的24名生物学亲属中有11人也被发现有该标记染色体。这个家族已知的谱系涵盖6代人,其中有证据表明有10例阿尔茨海默型痴呆症。痴呆症的平均发病年龄为65.8±5.5岁;明显受影响者的平均死亡年龄为74.9±8.3岁。一种新的风险评估模型被应用于该家族数据。发现这个家族中有该标记染色体的人患痴呆症的可能性是没有该标记染色体的人的4倍,这种风险的95%置信区间为1 - 50。痴呆症与该标记染色体之间的关联仅由偶然因素导致的概率为0.05(20分之一)。