Research Article

Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency

Table 4

G6PD levels categorized by the genotype of G6PD mutations and clinical phenotypes of 73 affected males and 27 heterozygous females.

Genotype of G6PD mutationG6PD level categorized by clinical phenotype (IU/ml.RBC) (mean±SD (min–max))
Neonatal JaundiceAcute hemolytic anemia
Affected male (66)Heterozygous female (24)Affected male (7)Heterozygous female (3)

Viangchan16.8 ± 9.6 (5–45)125.2 ± 53.7 (61–189)8148
Canton12.3 ± 8.2 (3–26)123.7 ± 76 (85–195)384
Kaiping11.8 ± 11.3 (7–34)9, 129, 18012, 25-
Mahidol11.75 ± 4.5 (8–17)108, 136109
Quing Yan13100, 152, 177
Aures103
Coimbra3423
Songklanagarind3, 28
Union109
Valladolid76159
Chinese-525
Mediterranean15
G6PD level (IU/ml.RBC) (mean±SD (min–max))17.26 ± 11.7 (3–76)136.1 ± 44.6 (9–195)11.8 ± 8.9 (3–25)113.7 ± 32.2 (84–148)

Data shown as mean+_SD or number (percent).