Acute Haemolysis Precipitating Rhabdomyolysis and Acute Kidney Injury in a Newly Diagnosed G6PD Deficiency: A Case Report

Authors

  • Jayne Ong Ai Xin Department of Paediatrics, Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia
  • Mardhiah Majid Department of Paediatrics, Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia
  • Husaini Utama Department of Paediatrics, Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia
  • Fahisham Taib Department of Paediatrics, Hospital Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia

DOI:

https://doi.org/10.3329/bjms.v21i3.59592

Keywords:

Glucose-6-phosphate, G6PD

Abstract

Glucose-6-phosphate dehydrogenase deficiency (G6PD) is a common X-linked genetic condition among Malaysians that have largely caused acute intravascular haemolysis. In G6PD deficient children, the phenomenon of rhabdomyolysis and myoglobinuria is a rare complication as muscle has more resistant to undergo acute myolysis. A 22-month-old Malay child was presented with severe anaemia following with ingestion of large amount of fava beans. He then developed into acute kidney injury together with the laboratory findings of intravascular haemolysis, rhabdomyolysis, and the presence of multi-systems bloods derangement. He showed positive response to hyperhydration, haemodialysis and blood transfusions.

Bangladesh Journal of Medical Science Vol. 21 No. 03 July’22 Page: 741-744

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Published

2022-05-21

How to Cite

Ai Xin, J. O. ., Majid, M. ., Utama, H. ., & Taib, F. . (2022). Acute Haemolysis Precipitating Rhabdomyolysis and Acute Kidney Injury in a Newly Diagnosed G6PD Deficiency: A Case Report. Bangladesh Journal of Medical Science, 21(3), 741–744. https://doi.org/10.3329/bjms.v21i3.59592

Issue

Vol. 21 No. 3 (2022)

Section

Case Reports

License

Copyright (c) 2022 Jayne Ong Ai Xin, Mardhiah Majid, Husaini Utama, Fahisham Taib

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