Walker D A, Harper P S, Newcombe R G, Davies K
J Med Genet. 1983 Feb;20(1):12-7. doi: 10.1136/jmg.20.1.12.
A study of mutation, biological fitness, and patterns of family building in Huntington's chorea has been carried out, based on a previously reported population study of the disorder in South Wales. No unequivocal new mutation was identified among 101 kindreds containing 418 affected persons, which supports the extreme rarity of mutation in this disorder. Increased values of fertility and fitness were found, both in relation to unaffected relatives and to the general population of the area. The proportion of unmarried persons and pattern of family building was comparable in affected and unaffected subjects, and no correlation with age at onset or mode of clinical presentation could be found.
基于此前报道的南威尔士该疾病的人群研究,开展了一项关于亨廷顿舞蹈症的突变、生物学适应性及家庭组建模式的研究。在包含418名患者的101个家族中,未发现明确的新突变,这支持了该疾病突变极为罕见的观点。在与未患病亲属及该地区普通人群的对比中,均发现生育力和适应性增加。未婚者比例及家庭组建模式在患病和未患病个体中相当,且未发现与发病年龄或临床表现方式存在关联。