Glucose-6-phosphate dehydrogenase (G6PD)-deficient infants: Enzyme activity and gene variants as risk factors for phototherapy in the first week of life

Author:

Wong Fei-Liang1,Ithnin Azlin2,Othman Ainoon3,Cheah Fook-Choe1

Affiliation:

1. Department of Paediatrics; Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre; Kuala Lumpur Malaysia

2. Department of Pathology; Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre; Kuala Lumpur Malaysia

3. Faculty of Medicine and Health Sciences; Universiti Sains Islam Malaysia; Nilai Malaysia

Funder

Fundamental Research Grant Scheme

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis;Nkhoma;Blood Cells Mol. Dis.,2009

2. Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: Prevalence among 1,286,000 Greek newborn infants;Missiou-Tsagaraki;J. Pediatr.,1991

3. Semiquantitative screening test for G6PD deficiency detects severe deficiency but misses a substantial proportion of partially-deficient females;Ainoon;Southeast Asian J. Trop. Med. Public Health,2003

4. Glucose-6-phosphate dehydrogenase deficiency neonatal screening: Preliminary evidence that a high percentage of partially deficient female neonates are missed during routine screening;Reclos;J. Med. Screen.,2000

5. Glucose-6-phosphate dehydrogenase deficiency;WHO Working Group;Bull. World Health Organ.,1989

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