Rouabhi F, Lapouméroulie C, Amselem S, Krishnamoorthy R, Adjrad L, Girot R, Chardin P, Benabdji M, Labie D, Beldjord C
Centre National de Transfusion Sanguine, CHU Mustapha, Alger, Algeria.
Hum Genet. 1988 Aug;79(4):373-6. doi: 10.1007/BF00282180.
An evaluation of beta thalassaemia mutations and the associated chromosomal haplotypes has been made among Algerian thalassaemic patients in this extended series. The major features of our findings are: (i) due to elevated proportion of consanguinity, the frequency of true homozygotes for a defect is high; (ii) Despite this high homozygosity within families, the number of molecular defects resulting in beta thalassaemia are very heterogeneous within this population. This is exemplified not only by the high heterogeneity of haplotypes and associated mutations, but also by the definition of several new haplotypes, among which two of them were found to be associated with novel mutations. Family studies have been performed in parallel to evaluate the degree of feasibility of antenatal diagnosis in this population.
在这个扩大的队列中,我们对阿尔及利亚地中海贫血患者的β地中海贫血突变及相关染色体单倍型进行了评估。我们研究结果的主要特点是:(i)由于近亲结婚比例升高,缺陷纯合子的频率很高;(ii)尽管家族内纯合性很高,但导致β地中海贫血的分子缺陷在该人群中非常异质。这不仅体现在单倍型和相关突变的高度异质性上,还体现在几种新单倍型的确定上,其中两种被发现与新突变相关。同时进行了家系研究,以评估该人群中产前诊断的可行性程度。