Mutation screening of phenylketonuria in the Far East of Russia

• Published in: Journal of human genetics Vol. 44; no. 6; pp. 368 - 371
• Main Authors: Sueoka, H, Moshinetsky, A, Nagao, M, Chiba, S
• Format: Journal Article
• Language: English
• Published: England 01.01.1999
• Subjects: Child; Child, Preschool; Genetic Testing; Humans; Infant; Mutation; Phenylalanine Hydroxylase - genetics; Phenylketonurias - genetics; Russia; Russia
• ISSN: 1434-5161; 1435-232X
• DOI: 10.1007/s100380050180

We analyzed mutant genotypes at the human phenylalanine hydroxylase (PAH) locus among phenylketonuria (PKU) patients in the Far East of Russia. A total of 60 variant alleles from 30 PKU families were analyzed for prevalent Caucasian mutations and restriction fragment length polymorphism/variable number of tandem repeats (RFLP/VNTR) haplotypes. Seventy-eight percent of all variant alleles carried six mutations. The most prevalent mutation was R408W (63%), with a haplotype background of 2.3. It also showed a very high degree of homozygosity (43%). The other five mutations (R158Q, R261Q, R252W, R261X, and IVS12nt-1) accounted for 1.7%-6.7% of all PKU alleles, and a single haplotype was associated with each genotype, except for R261Q. The genetic structure of PKU patients in the Far East of Russia seems to be relatively homogeneous, compared with that in the other Slavic and Oriental populations of surrounding countries. Prediction of a clinical phenotype and carrier detection will be feasible using DNA tests.