Kleijer Wim J, Laugel Vincent, Berneburg Mark, Nardo Tiziana, Fawcett Heather, Gratchev Alexei, Jaspers Nicolaas G J, Sarasin Alain, Stefanini Miria, Lehmann Alan R
Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
DNA Repair (Amst). 2008 May 3;7(5):744-50. doi: 10.1016/j.dnarep.2008.01.014. Epub 2008 Mar 10.
Laboratory diagnosis for DNA repair diseases has been performed in western Europe from the early seventies for xeroderma pigmentosum (XP) and from the mid-eighties for Cockayne syndrome (CS) and trichothiodystrophy (TTD). The combined data from the DNA repair diagnostic centres in France, (West) Germany, Italy, the Netherlands and the United Kingdom have been investigated for three groups of diseases: XP (including XP-variant), CS (including XP/CS complex) and TTD. Incidences in western Europe were for the first time established at 2.3 per million livebirths for XP, 2.7 per million for CS and 1.2 per million for TTD. As immigrant populations were disproportionately represented in the patients' groups, incidences were also established for the autochthonic western European population at: 0.9 per million for XP, 1.8 per million for CS and 1.1 per million for TTD. Perhaps contrary to general conceptions, compared to XP the incidence of CS appears to be somewhat higher and the incidence of TTD to be quite similar in the native West-European population.
自20世纪70年代初起,西欧就开始对着色性干皮病(XP)进行DNA修复疾病的实验室诊断,自80年代中期起开始对科凯恩综合征(CS)和毛发硫营养不良症(TTD)进行相关诊断。法国、(西)德 国、意大利、荷兰和英国的DNA修复诊断中心针对三组疾病(XP(包括XP变异型)、CS(包括XP/CS复合体)和TTD)的综合数据进行了研究。西欧地区XP、CS和TTD的发病率首次确定为每百万活产儿中分别有2.3例、2.7例和1.2例。由于移民人口在患者群体中所占比例过高,因此也确定了西欧本地人口的发病率:XP为每百万中有0.9例,CS为每百万中有1.8例,TTD为每百万中有1.1例。也许与一般观念相反,在西欧本地人口中,与XP相比,CS的发病率似乎略高,而TTD的发病率则与之相当。