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

Hypoplastic coronary arteries in a child with a mutation in Notch1: A case report.

Medicine - 14 Aug 2020

Shi Xiaoqing, Liu Jianxin, Wu Jinlin, Hua Yimin, Zhou Kaiyu, Li Yifei

Abstract excerpt

RATIONALE: Coronary artery abnormalities are usually of major significance in clinical cardiology and cardiac surgery departments due to associated myocardial ischemia, myocardial infarction, and sudden cardiac death. Among them, anatomical malformations account for most coronary artery abnormalities. However, hypoplasia of the coronary artery is a rare type of coronary artery without any genetic screening...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Computed Tomography Angiography
Share to Heart Transplantation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Receptor, Notch1

Source

Open in PubMed Open full text

Identifiers

PMID: 32871987
DOI: 10.1097/MD.0000000000021355
PMCID: PMC7437781

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

Hypoplastic coronary arteries in a child with a mutation in Notch1: A case report.PMID 32871987Read ↗

Expanding the cardiac spectrum of Noonan syndrome with RIT1 variant: Left main coronary artery atresia causing sudden death.Semantic proximity Read ↗

A Noonan-like pediatric patient with a de novo CBL pathogenic variant and an RNF213 polymorphism p.R4810K presenting with cardiopulmonary arrest due to left main coronary artery ostial atresia.Semantic proximity Read ↗

Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report.Semantic proximity Read ↗

Incidence of Congenital Anomalies of the Coronary Arteries in Embalmed CadaversSemantic proximity Read ↗

Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.Semantic proximity Read ↗

Reshaping Clinical Destiny of Silent ALCAPA: Multimodal Imaging-Driven Early Diagnosis and Mandatory InterventionSemantic proximity Read ↗

Molecular and cellular insights into the pathogenesis of coronary artery ectasia.Semantic proximity Read ↗

Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.Semantic proximity Read ↗

Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease.Semantic proximity Read ↗

Multimodality Imaging-Guided Diagnosis and Management of a Rare Coronary Artery Fistula with Coexistent Left Ventricular Noncompaction CardiomyopathySemantic proximity Read ↗

Two Cases of Anomalous Origin of Left Coronary Artery From The Pulmonary ArterySemantic proximity Read ↗

Coronary microvascular dysfunction: Phenotype-specific targeted therapies.Semantic proximity Read ↗

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