Title

Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections

UMMS Affiliation

Department of Pediatrics

Date

3-2004

Document Type

Article

Medical Subject Headings

Amino Acid Substitution; Anemia; Base Sequence; Blood Cells; Child; DNA; DNA, Complementary; Gene Expression; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Granulomatous Disease, Chronic; Humans; Infection; Male; Molecular Sequence Data; Polymorphism, Single-Stranded Conformational; Superoxides

Disciplines

Hematology | Oncology | Pediatrics

Abstract

Patients with severe leukocyte G6PD deficiency may present with impairment of NADPH oxidase activity and a history of recurrent infections, mimicking the phenotype of chronic granulomatous disease. We report herein a child with recurrent infections who initially received the diagnosis of G6PD deficiency. His erythrocyte G6PD activity was reduced: 1.8 U/g Hb (normal: 12.1 +/- 2.1 U/g Hb). Further studies revealed that G6PD activity in neutrophils, mononuclear leukocytes, and Epstein-Barr virus-transformed B-lymphocytes from the proband was similar to healthy controls. Molecular studies showed that the G6PD deficiency was due a 202 G-->A mutation, the A- variant common in African ethnic groups. The proband also exhibited severely impaired respiratory burst activity, as observed in X-linked CGD. Sequence analysis of genomic DNA showed a 264 G-->A substitution at the 3' splice junction of gp91-phox exon 3. The cDNA sequence showed a deletion of gp91-phox exon 3, giving rise to an unstable or nonfunctional mutant gp91-phox and to the phenotype of X-linked CGD. We propose that clinicians treating a patient with G6PD deficiency during a severe infection episode consider the possibility of temporary or permanent impairment of the phagocytes' microbicidal activity and the eventual association of G6PD deficiency and chronic granulomatous disease.

Rights and Permissions

Citation: Am J Hematol. 2004 Mar;75(3):151-6. doi: 10.1002/ajh.10477

Related Resources

Link to article in PubMed

PubMed ID

14978696