Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

The Arch of Aorta01:10

The Arch of Aorta

The coronary arteries, originating from the ascending aorta, bifurcate from two sinuses located within the ascending aorta. Positioned just above the aortic semilunar valve, these sinuses house essential aortic baroreceptors and chemoreceptors, crucial for maintaining cardiac function. The left coronary artery and the right coronary artery branch off from the left posterior and anterior aortic sinuses, respectively.
Encircling the heart, the coronary arteries form a ring-like structure before...
Aneurysm I: Introduction01:30

Aneurysm I: Introduction

An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
Thoracic Aorta01:15

Thoracic Aorta

The thoracic section of the aorta begins at the T5 vertebra and extends to the T12 level at the diaphragm, initially progressing through the mediastinum to the left of the spinal column. Throughout its course in the thoracic segment, the thoracic aorta emits various offshoots known collectively as visceral and parietal branches. The branches that predominantly supply blood to visceral organs are termed visceral branches and include bronchial, pericardial, esophageal, and mediastinal arteries,...
The Aorta01:14

The Aorta

The aorta is the largest artery in the human body. It originates from the left ventricle of the heart and extends down to the abdomen, where it splits into two smaller arteries. Structurally, it can be divided into four main parts: the ascending aorta, the aortic arch, the thoracic aorta, and the abdominal aorta.
The average diameter of the aorta is approximately 2-3 cm, but the size can vary depending on the section of the aorta and the individual's age, sex, and body size. The aorta is...
Abdominal Aorta01:25

Abdominal Aorta

Once the aorta traverses the diaphragmatic plane at the aortic hiatus, it is known as the abdominal aorta. This anatomical structure is positioned leftward of the spinal column, encased within a cocoon of adipose tissue behind the peritoneal cavity. It terminates at the L4 vertebra, where it splits into the common iliac arteries. Prior to this bifurcation, the abdominal aorta gives rise to several vital branches.
The celiac trunk, a singular artery, divides into the left gastric artery, which...
Aneurysm II: Clinical Manifestations and Diagnostic Studies01:21

Aneurysm II: Clinical Manifestations and Diagnostic Studies

Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Double trouble: double aortic arch with bilateral interruption and bilateral arterial ducts.

Cardiology in the young·2026
Same author

Effect of Valved Versus Non-valved Conduits on Ventricular Size and Function in Stage I Palliation for Hypoplastic Left Heart Syndrome.

Pediatric cardiology·2026
Same author

Impact of hypoplastic left heart syndrome anatomic subtype on mortality, ventricular function, and atrioventricular valve function in the current era.

JTCVS open·2026
Same author

Fibroinflammatory Diseases of Aorta: The Inside Look.

Aorta (Stamford, Conn.)·2026
Same author

Health-Related Quality of Life in Children with Hypoplastic Left Heart Syndrome: Changes over Time and Associations with Neurodevelopmental and Clinical Factors.

The Journal of pediatrics·2025
Same author

Neurodevelopmental Outcomes in Early Adolescence: The Pediatric Heart Network's Single Ventricle Reconstruction Trial.

Circulation·2025
Same journal

Context-Driven Management of Bilateral Diaphragmatic Failure After Phrenic Nerve Sacrifice.

The Annals of thoracic surgery·2026
Same journal

Uncomplicated type B aortic dissection: Are US-based societal guidelines delaying science?

The Annals of thoracic surgery·2026
Same journal

Methodological Paradigms and Clinical Realities in Defining High-Volume Centres for Valve-Sparing Aortic Root Replacement.

The Annals of thoracic surgery·2026
Same journal

Long-Term Outcomes of Concomitant Atrial Fibrillation Management During CABG: Standardization or Compromise?

The Annals of thoracic surgery·2026
Same journal

Ongoing Dialogue and Support for the Future of Congenital Cardiac Surgery.

The Annals of thoracic surgery·2026
Same journal

A Bridge With Gaps.

The Annals of thoracic surgery·2026
See all related articles

Related Experiment Video

Updated: May 16, 2026

Visualization and Analysis of Pharyngeal Arch Arteries using Whole-mount Immunohistochemistry and 3D Reconstruction
10:02

Visualization and Analysis of Pharyngeal Arch Arteries using Whole-mount Immunohistochemistry and 3D Reconstruction

Published on: March 31, 2020

Hypoplastic right cervical aortic arch.

Rabin Gerrah1, Amee Shah, Stephen M Langley

  • 1Pediatric Cardiac Surgery, Department of Surgery, Oregon Health and Science University, Doernbecher Children's Hospital, Portland, Oregon 97239, USA. gerrah@ohsu.edu

The Annals of Thoracic Surgery
|November 27, 2012
PubMed
Summary
This summary is machine-generated.

A rare congenital aortic anomaly in a neonate, featuring a hypoplastic, cervical, right-sided aortic arch, was successfully treated. Two surgical procedures, the Norwood and Rastelli, achieved a two-ventricular repair, overcoming significant diagnostic and surgical challenges.

More Related Videos

Left Atrial Ligation in the Avian Embryo as a Model for Altered Hemodynamic Loading During Early Vascular Development
04:37

Left Atrial Ligation in the Avian Embryo as a Model for Altered Hemodynamic Loading During Early Vascular Development

Published on: June 16, 2023

Novel and Innovative Hybrid Technique for Type A Aortic Dissection
06:26

Novel and Innovative Hybrid Technique for Type A Aortic Dissection

Published on: March 28, 2025

Related Experiment Videos

Last Updated: May 16, 2026

Visualization and Analysis of Pharyngeal Arch Arteries using Whole-mount Immunohistochemistry and 3D Reconstruction
10:02

Visualization and Analysis of Pharyngeal Arch Arteries using Whole-mount Immunohistochemistry and 3D Reconstruction

Published on: March 31, 2020

Left Atrial Ligation in the Avian Embryo as a Model for Altered Hemodynamic Loading During Early Vascular Development
04:37

Left Atrial Ligation in the Avian Embryo as a Model for Altered Hemodynamic Loading During Early Vascular Development

Published on: June 16, 2023

Novel and Innovative Hybrid Technique for Type A Aortic Dissection
06:26

Novel and Innovative Hybrid Technique for Type A Aortic Dissection

Published on: March 28, 2025

Area of Science:

  • Cardiovascular Surgery
  • Pediatric Cardiology
  • Congenital Heart Disease

Background:

  • Congenital anomalies of the aortic arch are rare and can present complex surgical challenges.
  • A hypoplastic, cervical, and right-sided aortic arch is an exceptionally uncommon presentation.

Observation:

  • A neonate presented with a rare congenital anomaly involving a hypoplastic aortic arch that was both cervical and right-sided.
  • This complex anatomical variation posed significant diagnostic and surgical hurdles.

Findings:

  • The neonate underwent a two-stage surgical repair, initially a Norwood procedure for right-sided arch reconstruction.
  • A subsequent Rastelli procedure completed the two-ventricular repair, effectively addressing the complex aortic anomaly.

Implications:

  • This case highlights successful surgical strategies for managing extremely rare aortic arch anomalies.
  • The described approach offers insights into achieving biventricular repair in complex congenital heart disease.
  • Effective management requires meticulous diagnostic evaluation and tailored surgical intervention.