Dianzani I, Farinasso L, Fortina P, Camaschella C, Ponzone R, Dahl H H, Cotton R G, Ponzone A
Department of Biomedical Sciences and Human Oncology, University of Turin, Italy.
J Inherit Metab Dis. 1989;12(2):162-5. doi: 10.1007/BF01800721.
Different mutations of the phenylalanine hydroxylase (PAH) gene leading to phenylketonuria (PKU) have been described associated with specific haplotypes in several European countries. In order to investigate the distribution of DNA haplotypes in Italy, restriction fragment length polymorphism (RFLP) analysis of the PAH gene was performed in nine Italian PKU patients from eight unrelated families, and in the available relatives. The analysis of eight polymorphic sites revealed haplotypes 1 and 6 in association with PKU. This pattern appears to differ from those reported for other European populations. The majority of the 14 PKU subjects studied showed compound heterozygosity for different haplotypes, as observed for other European series. RFLP analysis at the PAH locus allowed us to offer the possibility of prenatal diagnosis to six of the studied families. One prenatal diagnosis was performed and a normal fetus was diagnosed.
在几个欧洲国家,已描述了导致苯丙酮尿症(PKU)的苯丙氨酸羟化酶(PAH)基因的不同突变与特定单倍型相关。为了研究意大利DNA单倍型的分布情况,对来自8个无亲缘关系家庭的9名意大利PKU患者及其现有亲属进行了PAH基因的限制性片段长度多态性(RFLP)分析。对8个多态性位点的分析揭示了与PKU相关的单倍型1和单倍型6。这种模式似乎与其他欧洲人群的报道不同。在所研究的14名PKU受试者中,大多数显示出不同单倍型的复合杂合性,这与其他欧洲系列研究中观察到的情况相同。PAH基因座的RFLP分析使我们能够为6个研究家庭提供产前诊断的可能性。进行了一次产前诊断,诊断出胎儿正常。