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

Bacille Calmette-Guérin lymphadenitis and recurrent oral candidiasis in an infant with a new mutation leading to interleukin-12 receptor beta-1 deficiency.

Journal of investigational allergology & clinical immunology - 1 Jan 2011

Aytekin C, Dogu F, Tuygun N, Tanir G, Guloglu D, Boisson-Dupuis S, Bustamante J, Feinberg J, Casanova J L, Ikinciogullari A

Abstract excerpt

Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare syndrome characterized by predisposition to infections caused by weakly virulent mycobacteria, such as those in bacille Calmette-Guérin (BCG) vaccine and environmental mycobacteria. Salmonellosis has been reported in almost half of affected patients. Patients are also vulnerable to Mycobacterium tuberculosis infection. Several other infectious...

Read the complete abstract on PubMed

Topics

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

Share to BCG Vaccine
Share to Candidiasis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mycobacterium bovis

Share to Receptors, Interleukin-12

Share to Recurrence

Share to Salmonella Infections

Share to Skin Tests

Share to Tuberculosis

Source

Open in PubMed Open full text

Identifiers

PMID: 21905505
PMCID: PMC3361897

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

Bacille Calmette-Guérin lymphadenitis and recurrent oral candidiasis in an infant with a new mutation leading to interleukin-12 receptor beta-1 deficiency.PMID 21905505Read ↗

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.Semantic proximity Read ↗

Disseminated Salmonellosis in a child with IL12Rß1 deficiency – Case report and review of literature.Semantic proximity Read ↗

Severe Enteropathy and Hypogammaglobulinemia Complicating Refractory Mycobacterium tuberculosis Complex Disseminated Disease in a Child with IL-12Rβ1 Deficiency.Semantic proximity Read ↗

Clinical and genetic features of IL12Rb1 deficiency: Single center experience of 18 patients.Semantic proximity Read ↗

IL12Rβ1 defect presenting with massive intra-abdominal lymphadenopathy due to Mycobacterium intracellulare infection.Semantic proximity Read ↗

Disseminated Salmonellosis and cutaneous vasculitis in a child with IL12Rß1 deficiency – a case report & review of literature.Semantic proximity Read ↗

[Mendelian susceptibility to mycobacterial disease: a case report of disseminated infection due to Mycobacterium avium].Semantic proximity Read ↗

Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds.Semantic proximity Read ↗

The Child with Recurrent Mycobacterial Disease.Semantic proximity Read ↗

Severe BCG-osis Misdiagnosed as Multidrug-Resistant Tuberculosis in an IL-12Rβ1-Deficient Peruvian Girl.Semantic proximity Read ↗

[Primary immunodeficiency complicated with Bacillus Calmette-Guerin infection: identification and clinical phenotype of a case of novel interleukin-12Rbeta1 gene mutation].Semantic proximity Read ↗

Infectious diseases, autoimmunity and midline defect in a patient with a novel bi-allelic mutation in IL12RB1 gene.Semantic proximity Read ↗

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