The Elusive Cases of Carrier Females and G6PD Deficiency

Authors

  • Zahra Rashid Khan Yusra Medical and Dental College, Islamabad
  • Nasira Shaheen Combined Military Hospital, Abbotabad,
  • Nadir Ali Combined Military Hospital, Peshawar

Keywords:

Glucose 6 Phosphate Dehydrogenase, Dye Reduction Test.

Abstract

Objective: To screen newborn population for G6PD deficiency and compare results of the Dye Reduction
Test (DRT) with Quantitative estimation of G6PD deficiency.
Study Design: Cross-sectional study at Haematology Department, Army Medical College, National
University of Sciences and Technology and Military Hospital, Rawalpindi, (January-August, 2011)
Methodology: Cord blood (2.5 ml blood in K3EDTA bottle) samples were obtained from 120 newborns
after informed consent from parents. 65 patients were males and 55, females. Samples were evaluated
for G6PD deficiency using qualitative (DRT) and quantitative spectrophotometric technique. Data obtained
was analyzed using SPSS Windows version 17.
Results: Frequency of G6PD deficient cases was 2.5% by DRT and 4.2% by quantitative estimation.DRT
misclassified 2 cases of partial deficiency as normal in female population.
Conclusion: DRT has a diagnostic accuracy of 98.3 %, is specific, cost effective and easy to perform.
However, heterozygote female detection continues to be a challenge with this technique.

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Published

2018-11-17

Issue

Section

Original article

How to Cite

1.
Khan ZR, Shaheen N, Ali N. The Elusive Cases of Carrier Females and G6PD Deficiency. Int J Pathol [Internet]. 2018 Nov. 17 [cited 2024 Nov. 24];:30-6. Available from: https://jpathology.com/index.php/OJS/article/view/155