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

Autoimmune cytopenias in the 22q11.2 deletion syndrome

20 May 2003

Abstract excerpt

We describe two cases of recurrent autoimmune cytopenias, which were subsequently diagnosed with a 22q11.2 deletion/DiGeorge syndrome. The cases are of particular interest as both possessed limited clinical features of this syndrome, and the investigation of haematological abnormalities led to the establishment of a definitive genetic diagnosis.

Read the complete abstract on PubMed

Topics

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

Share to Cardiac Valve Diseases and Treatments
Share to Congenital heart defects research
Share to Infective Endocarditis Diagnosis and Management

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

Source

Identifiers

PMID: 12755799
DOI: 10.1046/j.1365-2257.2003.00508.x

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.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Autoimmune cytopenias in the 22q11.2 deletion syndromePMID 12755799Read ↗

Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome)Semantic proximity Read ↗

Evans Syndrome in a Patient with Chromosome 22q11.2 Deletion Syndrome: A Case ReportSemantic proximity Read ↗

The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndromeSemantic proximity Read ↗

Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)Semantic proximity Read ↗

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)Semantic proximity Read ↗

Longitudinal Analysis of Lymphocyte Function and Numbers in the First Year of Life in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)Semantic proximity Read ↗

Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)Semantic proximity Read ↗

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases.Semantic proximity Read ↗

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