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

[An exceptional component C3 deficiency revealed by serum protein electrophoresis].

Annales de biologie clinique - 1 Jan 2000

Dejoie T, Audrain M, Bach-Ngohou K, Denis M, Legoue-Morillon S, Thomas C, Masson D

Abstract excerpt

We report the case of a 5-years old child referred to the pediatric clinic due to a prolonged history of recurrent otitis. Initial immunologic investigation was normal but a severe C3 complement deficiency was detected by the absence of beta 2-globulin protein fraction using serum protein capillary electrophoresis. C3 was not detected in serum and total complement haemolytic activity was decreased. His mother and...

Read the complete abstract on PubMed

Topics

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

Share to Leukocyte Count
Share to Blood Proteins
Share to Complement C3

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Heterozygote

Share to Immunoglobulins

Share to Lymphocyte Count

Share to Recurrence

Share to Reference Values

Source

Identifiers

PMID: 19939777
DOI: 10.1684/abc.2009.0387

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[An exceptional component C3 deficiency revealed by serum protein electrophoresis].PMID 19939777Read ↗

Case Report: A novel homozygous splice-site variant in the C3 gene causing complete complement C3 deficiency in two unrelated Moroccan patients.Semantic proximity Read ↗

The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency.Semantic proximity Read ↗

Clinical laboratory standard capillary protein electrophoresis alerted of a low C3 state and lead to the identification of a Factor I deficiency due to a novel homozygous mutation.Semantic proximity Read ↗

Hereditary Deficiency of C3 in Animals and HumansSemantic proximity Read ↗

[STAT3 mutation in a child with hyper-IgE syndrome and incomplete clinical features].Semantic proximity Read ↗

Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency.Semantic proximity Read ↗

[Clinical findings and genetic bases of congenital complement deficiencies].Semantic proximity Read ↗

Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters.Semantic proximity Read ↗

Skipping of exon 27 in C3 gene compromises TED domain and results in complete human C3 deficiency.Semantic proximity Read ↗

[Combined-heterozygous deficiency of complement C7 in a patient with recurrent meningitis].Semantic proximity Read ↗

[Recurrent meningococcal infection in a young woman witha mutation in the C8B gene].Semantic proximity Read ↗

Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement.Semantic proximity Read ↗

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