Talk:Cardiovascular System - Double Outlet Right Ventricle

From Embryology
About Discussion Pages  
Mark Hill.jpg
On this website the Discussion Tab or "talk pages" for a topic has been used for several purposes:
  1. References - recent and historic that relates to the topic
  2. Additional topic information - currently prepared in draft format
  3. Links - to related webpages
  4. Topic page - an edit history as used on other Wiki sites
  5. Lecture/Practical - student feedback
  6. Student Projects - online project discussions.
Links: Pubmed Most Recent | Reference Tutorial | Journal Searches

Glossary Links

Glossary: A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | Numbers | Symbols | Term Link

Cite this page: Hill, M.A. (2019, June 17) Embryology Cardiovascular System - Double Outlet Right Ventricle. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Talk:Cardiovascular_System_-_Double_Outlet_Right_Ventricle

2019

Double-outlet right ventricle is not hypoplastic left heart syndrome

Nat Genet. 2019 Feb;51(2):198. doi: 10.1038/s41588-018-0324-4.

We write to express our concerns that the report ‘The complex genetics of hypoplastic left heart syndrome’ by Liu et al.(28530678) is misleading, and the data presented in the figures and in the Mouse Genome Informatics repository do not convincingly demonstrate hypoplastic left heart syndrome (HLHS).

Chaudhry B1, Henderson D2, Anderson R3. Author information PMID: 30617254 DOI: 10.1038/s41588-018-0324-4

Imaging Spectrum of Double-Outlet Right Ventricle on Multislice Computed Tomography

J Thorac Imaging. 2019 Feb 15. doi: 10.1097/RTI.0000000000000396. [Epub ahead of print]

Priya S1, Nagpal P1, Sharma A2, Pandey NN2, Jagia P2. Author information Abstract Double-outlet right ventricle is a complex congenital heart disease that encompasses various common and rare subtypes. Surgical management of these patients needs to be individualized owing to extremely variable morphology and hemodynamics. Imaging plays a crucial role in determination and characterization of outflow tract morphology. The assessment of ventricular septal defect routability with identification of associated anomalies has therapeutic implications in these patients. Multislice computed tomography with advanced 3-dimensional postprocessing techniques and dose-reduction strategies is invaluable in defining the anatomy and morphology of double-outlet right ventricle with simultaneous assessment of associated anomalies. PMID: 30801451 DOI: 10.1097/RTI.0000000000000396


2017

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

Int J Mol Med. 2017 Jan 20. doi: 10.3892/ijmm.2017.2865.

Li L1, Wang J2, Liu XY3, Liu H4, Shi HY4, Yang XX4, Li N4, Li YJ4, Huang RT5, Xue S5, Qiu XB4, Yang YQ4.

Abstract

Congenital heart defects (CHDs), a wide variety of developmental abnormalities in the structures of the heart and the great thoracic blood vessels, are the most common form of birth defect in humans worldwide. CHDs are accountable for substantial morbidity and are still the leading cause of birth defect‑related deaths. Recent studies have demonstrated the pivotal roles of genetic defects in the pathogenesis of CHDs, and a great number of genetic mutations have been associated with CHDs. Nevertheless, CHDs are a genetically heterogeneous disorder and the genetic basis underlying CHDs in an overwhelming majority of cases remains unclear. In the present study, the coding exons and flanking introns of the heart and neural crest derivatives expressed transcript 1 (HAND1) gene, which encodes a basic helix‑loop‑helix transcription factor crucial for cardiovascular development, were sequenced in 158 unrelated patients with CHDs, and a de novo heterozygous mutation, p.K132X, was identified in a patient with double outlet right ventricle (DORV), as well as ventricular septal defect. The nonsense mutation, which was predicted to produce a truncated HAND1 protein lacking 84 carboxyl‑terminal amino acids, was absent in 600 control chromosomes. Functional analyses revealed that the HAND1 K132X mutant had no transcriptional activity. Furthermore, the mutation disrupted the synergistic activation between HAND1 and GATA binding protein 4 (GATA4), another cardiac core transcription factor causally linked to CHDs. To the best of our knowledge, this is the first report on the association of HAND1 loss‑of‑function mutation with an enhanced susceptibility to DORV in humans. These findings expand the phenotypic spectrum linked to HAND1 mutations, suggesting potential implications for the development of novelo prophylactic and therapeutic strategies for DORV.

PMID 28112363 DOI: 10.3892/ijmm.2017.2865


Double-outlet right ventricle with an intact interventricular septum and concurrent hypoplastic left ventricle in a calf

J Vet Cardiol. 2017 Jan 19. pii: S1760-2734(16)30142-4. doi: 10.1016/j.jvc.2016.11.002.

Newhard DK1, Jung SW2, Winter RL1, Kuca T1, Bayne J1, Passler T1.

Abstract

A 3-day-old Hereford heifer calf presented for evaluation of lethargy and dyspnea, with persistent hypoxia despite supplemental oxygen therapy. A grade III/VI right apical systolic murmur was noted during cardiac auscultation. Echocardiography revealed a double-outlet right ventricle with an intact interventricular septum and concurrent hypoplastic left ventricle and tricuspid valve dysplasia. Post-mortem examination revealed additional congenital anomalies of ductus arteriosus, patent foramen ovale, and persistent left cranial vena cava. This report illustrates the use of echocardiographic images to diagnose a double-outlet right ventricle with an intact interventricular septum and a hypoplastic left ventricle in a calf. Copyright © 2016 Elsevier B.V. All rights reserved. KEYWORDS: Bovine; Congenital heart defect; Persistent hypoxia

PMID 28111139 DOI: 10.1016/j.jvc.2016.11.002