Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Severe G6PD deficiency leads to recurrent infections and defects in ROS production: Case report and literature review

24 Oct 2022

Abstract excerpt

Purpose: Severe glucose-6-phosphate dehydrogenase (G6PD) deficiency can lead to reduced nicotinamide adenine dinucleotide phosphate oxidase activity in phagocytes, resulting in immunodeficiency, with a limited number of reported cases. Here, we aimed to report a child with severe G6PD deficiency in China and investigate the mechanism of his recurrent infections. Methods: The clinical manifestations and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood disorders and treatments
Share to Neonatal Health and Biochemistry
Share to Neonatal Respiratory Health Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36353116
DOI: 10.3389/fgene.2022.1035673

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Severe G6PD deficiency leads to recurrent infections and defects in ROS production: Case report and literature reviewPMID 36353116Read ↗

Geographic Variability and Pathogen-Specific Considerations in the Diagnosis and Management of Chronic Granulomatous DiseaseSemantic proximity Read ↗

Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.Semantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase Deficiency.Semantic proximity Read ↗

Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.Semantic proximity Read ↗

Serum microRNAs as new biomarkers for detecting subclinical hemolysis in the nonacute phase of G6PD deficiencySemantic proximity Read ↗

Hematologically important mutations: X-linked chronic granulomatous disease (fourth update).Semantic proximity Read ↗

G6PD: Population genetics and clinical manifestationsSemantic proximity Read ↗

Seven chronic granulomatous disease cases in a single-center experience and a review of the literature.Semantic proximity Read ↗

Gene symbol: G6PD. Disease: Glucose-6-phosphate dehydrogenase deficiency.Semantic proximity Read ↗

Glucose-6-Phosphate Dehydrogenase: Update and Analysis of New Mutations around the World.Semantic proximity Read ↗

Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohort.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.