Midro A T
Zakładu Genetyki Klinicznej Instytutu Połoznictwa i Chorób Kobiecych, Ak. Med., Białymstoku.
Wiad Lek. 1992 Oct;45(19-20):775-80.
The principles are presented of genetic counselling for families with carrier state of reciprocal chromosome translocations (RCT). RCTs are the risk factor for the occurrence of reproduction disturbances, such as infertility, spontaneous abortion, congenital anomalies in the offsprings, and the degree of risk depends to a large extent on which chromosome segments are in the state of imbalance in the offsprings, due to various mechanisms of abnormal meiotic segregation. The uniqueness of chromosome translocations with respect to the type of chromosomes involved in translocations, and the location of breaking sites is the reason for the necessity of construing large pedigrees for the evaluation of the degree of risk. The newest Stene and Stengel-Rutkowski model makes possible the combination of smaller pedigrees in translocation groups of the so-called single risk of imbalance and determination of the individual risk of birth of children with anomalies. A number of psychological determinants are important for the possibility of genetic investigations in the affected families, and the decision about procreation may be influenced by a number of determinants other than the result of genetic counsel.
本文阐述了针对具有相互染色体易位(RCT)携带者状态家庭的遗传咨询原则。RCT是生殖障碍发生的风险因素,如不孕、自然流产、后代先天性异常,且风险程度在很大程度上取决于由于减数分裂异常分离的各种机制,后代中哪些染色体片段处于不平衡状态。染色体易位在涉及易位的染色体类型以及断裂位点位置方面的独特性,是为评估风险程度而构建大型系谱的必要性所在。最新的斯特内和施滕格尔 - 鲁特科夫斯基模型使得在所谓不平衡单一风险的易位组中合并较小系谱以及确定出生异常儿童的个体风险成为可能。许多心理因素对于受影响家庭进行基因调查的可能性很重要,并且生育决定可能受到基因咨询结果以外的许多因素影响。