[Characteristics of PAH gene variants among 113 phenylketonuria patients from Henan Province]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):791-795. doi: 10.3760/cma.j.issn.1003-9406.2018.06.003.
[Article in Chinese]

Abstract

Objective: To explore the characteristics of PAH gene variants among 113 phenylketonuria patients from Henan Province.

Methods: The 13 exons of the PAH gene were subjected to PCR amplification and direct sequencing. Large fragment deletion and duplication of the PAH gene were detected with a multiple ligation-dependent probe amplification (MLPA) assay.

Results: In total 195 point variants and 3 large fragment deletions were detected among the 226 alleles, with the detection rates being 86.28% and 1.33%, respectively. Variants of p.Arg243Gln (18.14%), p.Arg111X (6.19%), p.Arg53His (5.31%), EX6-96A>G (5.31%), p.Tyr356X (4.87%) and p.Val399Val (4.42%) were relatively common. Most of the variants were located in exons 7, 11, 3 and 6. Missense variations were most common. Four novel variations were detected, which included c.1016C>A (p.Ser339Tyr), c.1000T>C (p.Cys334Arg), c.1110G>T (p.Glu370Asp), and IVS6+1G>T.

Conclusion: The PAH gene variations in Henan Province have featured extensive allelic heterogeneity and variety.

MeSH terms

  • China
  • Exons
  • Humans
  • Mutation, Missense
  • Phenylalanine Hydroxylase / genetics*
  • Phenylketonurias / genetics*
  • Point Mutation
  • Sequence Deletion

Substances

  • Phenylalanine Hydroxylase