𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays

✍ Scribed by O. Ainoon; Y.H. Yu; A.L. Amir Muhriz; N.Y. Boo; S.K. Cheong; N.H. Hamidah


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
50 KB
Volume
21
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis


We performed DNA analysis using cord blood samples on 86 male Malay neonates diagnosed as G6PD deficiency in the National University of Malaysia Hospital by a combination of rapid PCR-based techniques, single-stranded conformation polymorphism analysis (SSCP) and DNA sequencing. We found 37.2% were 871G>A (G6PD Viangchan), 26.7% were nt 563 C>T (G6PD Mediterranean) and 15.1% were 487G>A (G6PD Mahidol) followed by 4.7% 1376G>T (G6PD Canton), 3.5% 383T>C (G6PD Vanua Lava), 3.5% 592C>T (G6PD Coimbra), 2.3% 1388G>A (G6PD Kaiping), 2.3% 1360C>T (G6PD Union), 2.3% 1003G>A (G6PD Chatham), 1.2% 131C>G (G6PD Orissa) and 1.2% 1361G>A (G6PD Andalus). Seventy-one (82.6%) of the 86 G6PD-deficient neonates had neonatal jaundice. Fifty seven (80%) of the 71 neonates with jaundice required phototherapy with only one neonate progressing to severe hyperbilirubinemia (serum bilirubin >340 micromol/l) requiring exchange transfusion. There was no significant difference in the incidence of neonatal jaundice, mean serum bilirubin level, mean age for peak serum bilirubin, percentage of babies requiring phototherapy and mean number of days of phototherapy between the three common variants. In conclusion, the molecular defects of Malay G6PD deficiency is heterogeneous and G6PD Viangchan, Mahidol and Mediterranean account for at least 80% of the cases. Our findings support the observation that G6PD Viangchan and Mahidol are common Southeast Asian variants. Their presence in the Malays suggests a common ancestral origin with the Cambodians, Laotians and Thais. Our findings together with other preliminary data on the presence of the Mediterranean variant in this region provide evidence of strong Arab influence in the Malay Archipelago.


πŸ“œ SIMILAR VOLUMES


Glucose-6-phosphate dehydrogenase (G6PD)
✍ O. Ainoon; J. Joyce; N.Y. Boo; S.K. Cheong; Z.A. Zainal; N.H. Hamidah πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 31 KB πŸ‘ 2 views

We screened 38 G6PD-deficient male Chinese neonates for known G6PD mutations using established PCR-based techniques. We found 50.0% (19 of 38) were mutation 1376G>T, 34.2% (13 of 38) were mutation 1388G>A, 5.2% (2 of 38 ) were mutation 95A>G and 2.2% (1 of 38) was mutation 1024C>T. In 7% (3 of 38) o

A new glucose 6 phosphate dehydrogenase
✍ Renzo Galanello; Daniela Loi; Carla Sollaino; Sandra DessΓ¬; Antonio Cao; Maria A πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 31 KB πŸ‘ 2 views

In this paper we report a male infant heterozygous for -thalassemia with a mild glucose 6 phosphate dehydrogenase deficiency. The molecular basis of this new Class III G6PD variant is a G->T mutation at nucleotide 34 in the exon 2, which predicts a Val->Leu aminoacid substitution at codon 12. We des

Two new glucose-6 phosphate dehydrogenas
✍ Dr. Naif S. Karadsheh; A. S. Awidi; M. S. Tarawneh πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 385 KB πŸ‘ 2 views

Two glucose-6-phosphate dehydrogenase (G6PD) variants were investigated. G6PD Amman-1 was partially purified from the red cells of a patient suffering from recurrent jaundice and spontaneous episodic attacks of severe hemolysis in the absence of oxidant drugs, infection, or fava beans. The enzymatic

Glucose-6-phosphate dehydrogenase (G6PD)
✍ I. Nuchprayoon; S. Sanpavat; S. Nuchprayoon πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 78 KB

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary disorder in humans. Through a population study for G6PD deficiency using a cord blood quantitative G6PD assay in Bangkok, Thailand, we found that the prevalence of G6PD deficiency is 11.1% in Thai male (N=350) and 5.8%