<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>38</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="epublish">
        <Year>2009</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Epidemiological and Clinical Study of Phenylketonuria (PKU) Disease in the National Screening Program of Neonates, Fars Province, Southern Iran</title>
    <FirstPage>58</FirstPage>
    <LastPage>64</LastPage>
    <AuthorList>
      <Author>
        <FirstName>S</FirstName>
        <LastName>Senemar</LastName>
        <affiliation locale="en_US">Human Genetics Research Group, Iranian Academic Center for Education, Culture &amp; Research (ACECR), Fa</affiliation>
      </Author>
      <Author>
        <FirstName>H</FirstName>
        <LastName>Ganjekarimi</LastName>
        <affiliation locale="en_US">Paramedical School of Shiraz University of medical science (SUMS), Iran</affiliation>
      </Author>
      <Author>
        <FirstName>M</FirstName>
        <LastName>Fathzadeh</LastName>
        <affiliation locale="en_US">Human Genetics Research Group, Iranian Academic Center for Education, Culture &amp; Research (ACECR), Fa</affiliation>
      </Author>
      <Author>
        <FirstName>S</FirstName>
        <LastName>Senemar</LastName>
        <affiliation locale="en_US">Center of Blood Transfusion of Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>B</FirstName>
        <LastName>Tarami</LastName>
        <affiliation locale="en_US">Dept. of Mathematics, Yasuj University, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>M</FirstName>
        <LastName>Bazrgar</LastName>
        <affiliation locale="en_US">Human Genetics Research Group, Iranian Academic Center for Education, Culture &amp; Research (ACECR), Fa</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Classic phenylketonuria (PKU) is a rare metabolic disorder that results from a deficiency of a liver enzyme known as phenylalanine hydroxylase (PAH). In this study, we researched about PKU epidemiological factors and health quality of patients after the neonatal screening program.
Methods: Neonatal screening for PKU was conducted by one neonatal screening center in Fars Province, in Shiraz Paramedical University. All Fars infants must refer only to this center, in which a heel prick blood sample&#xA0; of each infant was collected at 72 hours postnatal on to standard filter paper and asked questions from the children's parent's and the doctor examined the patients receiving phenylalanine- free milk through examining the children's development. PKU was screened by Fluorometric method.
Results: Totally of 70477 newborns screened for PKU, 15- cases of PKU detected with an incidence of 1:4698. In "Eghlid", that is a city in Fars Province. The prevalence of the disease is 1:382 of newly born babies. The frequency of familial marriage in these children's parents is 86.6%. Twenty nine percent of them were observed among those who had married their close relatives. Mean rate of normal development in PKU patients was 95%.
Conclusion: Consanguineous marriage is a major cause in that pattern particular in Iranian. The treatment of PKU after newborn screening is used. With special diet in above of 90% newborn is satisfactory. Now screening should be executed for all of family that they have familial history of PKU in Iran.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/3190</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/3190/2989</pdf_url>
  </Article>
</Articles>
