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Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil

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Phenylketonuria (PKU) is an autosomal recessive disease resulting from mutations in the PAH gene. Most of the patients are compound heterozygotes, and genotype is a major factor in determining the… Click to show full abstract

Phenylketonuria (PKU) is an autosomal recessive disease resulting from mutations in the PAH gene. Most of the patients are compound heterozygotes, and genotype is a major factor in determining the phenotypic variability of PKU. More than 1,000 variants have been described in the PAH gene. Rio de Janeiro's population has a predominance of Iberian, followed by African and Amerindian ancestries. It is expected that most PKU variants in this Brazilian state have originated in the Iberian Peninsula. However, rare European, African or pathogenic variants that are characteristic of the admixed population of the state might also be found.

Keywords: analysis pah; gene phenylketonuria; rio janeiro; mutation analysis; gene; pah gene

Journal Title: Molecular Genetics & Genomic Medicine
Year Published: 2018

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