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

Berry syndrome: a possible genetic link.

Pediatric cardiology - 1 Aug 2013

Jayaram Natalie, Knowlton Joshua, Shah Sanket, Gelatt Mark, Lofland Gary, Raghuveer Geetha

Abstract excerpt

Berry syndrome comprises a rare combination of heart defects that includes aortopulmonary window, interrupted aortic arch, intact ventricular septum, and aortic origin of the right pulmonary artery. We report the case of a neonate confirmed to have Berry syndrome by transthoracic echocardiogram and computed tomography (CT). This neonate had the additional finding of an aberrant right subclavian artery arising...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Aorta, Thoracic
Share to Diagnosis, Differential

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

Share to Echocardiography

Share to Heart Defects, Congenital

Share to Pulmonary Artery

Share to Syndrome

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 22790358
DOI: 10.1007/s00246-012-0412-7

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

Berry syndrome: a possible genetic link.PMID 22790358Read ↗

Bicuspid Aortic Valve: Genetic and Clinical InsightsSemantic proximity Read ↗

Isolated aberrant right subclavian artery: an underlying clue for genetic anomaliesSemantic proximity Read ↗

Genetic abnormalities in fetal congenital heart disease with aberrant right subclavian arterySemantic proximity Read ↗

Aberrant right subclavian artery: embryology, prenatal diagnosis and clinical significanceSemantic proximity Read ↗

Fetal double aortic arch: prenatal sonographic and postnatal computed tomography angiography features, associated abnormalities and clinical outcomesSemantic proximity Read ↗

Aberrant right subclavian artery: the importance of distinguishing between isolated and non-isolated cases in prenatal diagnosis and clinical managementSemantic proximity Read ↗

Prenatal Diagnosis, Associated Findings and Postnatal Outcome of Fetuses With Truncus Arteriosus Communis (TAC)Semantic proximity Read ↗

Fetal cardiac anomalies and genetic syndromesSemantic proximity Read ↗

Complete trisomy 9 with unusual phenotypic associations: Dandy-Walker malformation, cleft lip and cleft palate, cardiovascular abnormalities.Semantic proximity Read ↗

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

Quadricuspid aortic valve and anomalous systemic venous connection in a patient with cat-eye syndrome.Semantic proximity Read ↗

Prenatal diagnosis of Scimitar syndrome associated with duplicated superior vena cava in fetal echocardiography: A case reportSemantic proximity Read ↗

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