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

Case Report: Hemophagocytic Lymphocytosis in a Patient With Glutaric Aciduria Type IIC.

Frontiers in immunology - 1 Jan 2021

Huang Lingtong, Wu Wei, Zhu Yijing, Yu Huili, Tang Lingling, Fang Xueling

Abstract excerpt

Hemophagocytic lymphocytosis (HLH) is a rare disease caused by inborn errors of immunity (IEI), secondary to infection, lymphoma or autoimmune disorders, but we often overlook the fact that HLH can be secondary to inborn errors of metabolism (IEM). Here, we describe a patient who was diagnosed with glutaric aciduria type IIC complicated by features suggestive of possible HLH. The diagnosis of glutaric aciduria...

Read the complete abstract on PubMed

Topics

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

Share to Disease Susceptibility
Share to Electron-Transferring Flavoproteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Erythrocyte Indices

Share to Iron-Sulfur Proteins

Share to Lymphohistiocytosis, Hemophagocytic

Share to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Share to Oxidoreductases Acting on CH-NH Group Donors

Share to Tomography, X-Ray Computed

Source

Open in PubMed Open full text

Identifiers

PMID: 35095902
DOI: 10.3389/fimmu.2021.810677
PMCID: PMC8792439

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case Report: Hemophagocytic Lymphocytosis in a Patient With Glutaric Aciduria Type IIC.PMID 35095902Read ↗

Inborn Errors of MetabolismSemantic proximity Read ↗

An infant with glutaric aciduria type IIc diagnosed with a novel mutation.Semantic proximity Read ↗

Immune Dysregulation Syndrome Associated with Inborn Errors of Metabolism – Hemophagocytic Lymphohistiocytosis in the Context of Isovaleric Acidemia: A Case ReportSemantic proximity Read ↗

Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia.Semantic proximity Read ↗

Functional Overlap of Inborn Errors of Immunity and Metabolism Genes Define T Cell Immunometabolic VulnerabilitiesSemantic proximity Read ↗

Functional overlap of inborn errors of immunity and metabolism genes defines T cell metabolic vulnerabilitiesSemantic proximity Read ↗

A compound heterozygote case of glutaric aciduria type II in a patient carrying a novel candidate variant in ETFDH gene: A case report and literature review on compound heterozygote cases.Semantic proximity Read ↗

Gaucher Disease Coexisting with Cytomegalovirus Infection: A Rare Presentation in an Infant.Semantic proximity Read ↗

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).Semantic proximity Read ↗

Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A).Semantic proximity Read ↗

Acute Encephalopathy Caused by Inherited Metabolic DiseasesSemantic proximity Read ↗

The presence of white cell Jordan's anomaly in multiple Acyl-CoA dehydrogenase deficiency: A case report and implications for clinical practice.Semantic proximity Read ↗

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