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

22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil

29 May 2008

Abstract excerpt

The 22q11.2 deletion syndrome (22q11DS) is one of the most recognizable causes of congenital heart defects (CHDs), but the frequency varies in non-selected populations. The purpose of this study was to determine the incidence and clinical features of patients with CHD and 22q11DS admitted to a pediatric cardiology intensive care unit in Brazil. In a prospective study, we evaluated a consecutive series of 207...

Read the complete abstract on PubMed

Topics

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

Share to Congenital heart defects research
Share to Congenital Heart Disease Studies
Share to Genomic variations and chromosomal abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 18512234
DOI: 10.1002/ajmg.a.32378

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

22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in BrazilPMID 18512234Read ↗

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiersSemantic proximity Read ↗

The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population‐based studySemantic proximity Read ↗

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.Semantic proximity Read ↗

Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort studySemantic proximity Read ↗

Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).Semantic proximity Read ↗

Rare and Complex Cardiac Anomalies Associated with 22q11.2 Deletion: An Ultrasonographic Visual Trip from Diagnosis until DeliverySemantic proximity Read ↗

Clinical findings in 32 patients with 22qll.2 microdeletion attended in the city of Córdoba, Argentina.Semantic proximity Read ↗

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.Semantic proximity Read ↗

Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease.Semantic proximity Read ↗

22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype.Semantic proximity Read ↗

Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort.Semantic proximity Read ↗

An Overview of the Trajectory of Brazilian Individuals with 22q11.2 Deletion Syndrome Until Diagnosis.Semantic proximity Read ↗

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