Literature DB >> 24575273

G6PD Enzyme Deficiency in Neonatal Pathologic Hyperbilirubinemia in Yazd.

M Pahlavanzadeh1, S Hekmatimoghaddam2, M Teremahi Ardestani3, M Ghafoorzadeh4, Mm Aminorraaya5.   

Abstract

BACKGROUND: About 7.5% of the world population carries one or two deficient copy of glucose-6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 to 14.9%. This study aimed on determination of frequency of G6PD deficiency in neonates with jaundice who were hospitalized during 6 months (September 2008 to February 2009) in the city of Yazd, Iran.
MATERIALS AND METHODS: In this study, 105 icteric neonates in the hospitals of Yazd were evaluated. Data was collected from hospital records, and the G6PD activity was measured by photometric biochemical assay. Statistical analysis of data was performed by the SPSS-16 software, using Student's t-test and Pearson's chi-squared test.
RESULTS: Between all of studied neonates, 19 (18.1%) had G6PD deficiency, and consisted of 15 boys (29.4% of boys) and 4 girls (7.4% of girls). In 100% of cases, the jaundice began in the first week after birth. The average total serum bilirubin at hospitalization was 17.22 mg/dL. In 31.5% of the G6PD-defficient neonates, exchange transfusion became necessary, which is significantly more than the rate in G6PD-sufficient (4.6%) neonates (P-value<0.05).
CONCLUSION: In general, the frequency of G6PD deficiency in this study seems quite high. Regarding its severity and frequent need for exchange transfusion, we recommend that all of the icteric neonates should be evaluated for G6PD activity. Also, it is better to test for G6PD deficiency in all of the neonates, to detect its presence and to prevent its complications such as favism and oxidant drug-induced hemolysis, since the test has a low cost.

Entities:  

Keywords:  Bilirubin; Favism; Glucosephosphate Dehydrogenase Deficiency; Jaundice; Neonatal

Year:  2013        PMID: 24575273      PMCID: PMC3915450     

Source DB:  PubMed          Journal:  Iran J Ped Hematol Oncol        ISSN: 2008-8892


  6 in total

1.  Frequency of Mediterranean mutation among a group of Saudi G6PD patients in Western region-Jeddah.

Authors:  M A Gari; A G Chaudhary; M H Al-Qahtani; A M Abuzenadah; A Waseem; H Banni; F M Al-Sayes; A Al-Harbi; S Lary
Journal:  Int J Lab Hematol       Date:  2010-02       Impact factor: 2.877

2.  Epidemiology of neonatal jaundice at the University Hospital of the West Indies.

Authors:  C Henny-Harry; H Trotman
Journal:  West Indian Med J       Date:  2012-01       Impact factor: 0.171

3.  Glucose-6-phosphate dehydrogenase and red cell pyruvate kinase deficiency in neonatal jaundice cases in egypt.

Authors:  Mohammed Abdel Fattah; Eman Abdel Ghany; Alia Adel; Dalia Mosallam; Shahira Kamal
Journal:  Pediatr Hematol Oncol       Date:  2010-05       Impact factor: 1.969

4.  Evaluation of glucose-6-phosphate dehydrogenase deficiency without hemolysis in icteric newborns at Mazandaran province, Iran.

Authors:  Amir Hossein Ahmadi; Zeynab Ghazizadeh
Journal:  Pak J Biol Sci       Date:  2008-05-15

5.  Insertion/Deletion polymorphisms do play any role in G6PD deficiency individuals in the Kingdom of the Saudi Arabia.

Authors:  Khalid K Alharbi; Imran Ali Khan; Alaa Salem A Abed; Rabbani Syed
Journal:  Bioinformation       Date:  2013-01-09

6.  Neonatal hyperbilirubinemia in infants with G6PD c.563C > T Variant.

Authors:  Bushra Moiz; Amna Nasir; Sarosh Ahmed Khan; Saleema Amin Kherani; Maqbool Qadir
Journal:  BMC Pediatr       Date:  2012-08-20       Impact factor: 2.125

  6 in total
  1 in total

Review 1.  Etiology and therapeutic management of neonatal jaundice in Iran: a systematic review and meta-analysis.

Authors:  Yadollah Zahed Pasha; Shaghayegh Alizadeh-Tabari; Ermia Zahed Pasha; Mohammad Zamani
Journal:  World J Pediatr       Date:  2020-02-12       Impact factor: 2.764

  1 in total

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