Results 31 to 40 of about 4,910 (169)

Coronary Artery Bypass Grafting in a Patient With Multivessel Disease and Dextrocardia With Situs Inversus Totalis [PDF]

Texas Heart Institute Journal
Dextrocardia with situs inversus totalis is a rare hereditary condition characterized by reversed orientation of the major thoracic and abdominal organs.
Rohit Shahani, MD, Adham Ahmed, BS, Frank M. Rosell, MD, Alexander Iribarne, MD, MS   +3 more
doaj   +1 more source

Dextrocardia

Pediatría, 2023
Antecedentes: La dextrocardia es una malformación embriológica que está causada porque el tubo cardiaco primitivo se dobla a la izquierda en lugar de hacerlo hacia la derecha (1). Esta patología puede ser asintomática, mientras que en otras situaciones presenta sintomatología dependiendo de los defectos cardiacos asociados, la radiografía de tórax y la
Ibad Ur Rehman, Khadija Iqbal, Irfan Ullah   +2 more
openaire   +2 more sources

Complex adult congenital heart disease: A rare case of dextrocardia with double-outlet right ventricle

Nigerian Journal of Medicine, 2023
Double-outlet right ventricle (DORV) is a complex and rare congenital heart disease (CHD), which is usually symptomatic early in childhood and thus diagnosed early. Dextrocardia is another rare CHD that can occur either as an isolated cardiac abnormality
Adeola Olubunmi Ajibare, Oluwaseye Michael Oladimeji, Oluwafemi Tunde Ojo, Folasade Adeola Daniel, Philip Alaba Adebola, Abdulazeez Olanrewaju   +5 more
doaj   +1 more source

Heart on the right side: A rare case report of dextrocardia with situs solitus, L-TGA (levo-transposition of the great arteries) and single ventricle physiology [PDF]

Journal of Research in Clinical Medicine
Dextrocardia is a rare congenital anomaly characterized by the positioning of the heart towards the right side of the chest. The prevalence of dextrocardia with situs solitus is 1 in 30000 live births and 1 in 900000 in the adult population.
Gurusha Bahl, Md Sadique Hussain, Dinesh K Upadhyay, Narendra Meena, Rajveer Singh, Tekchand Narang   +5 more
doaj   +1 more source

Off-pump coronary artery bypass in poland syndrome with dextrocardia: case report

Journal of Cardiothoracic Surgery, 2011
Poland Syndrome is a congenital disorder characterised by hypoplasia of the pectoral muscles along with upper extremity deformities. We encountered a patient with Poland syndrome associated with dextrocardia and also failed pectus excavatum repairs who ...
More Ranjit, Srivastava Vivek, Tang Augustine   +2 more
doaj   +1 more source

CARDIAC STENTING IN DEXTROCARDIA- AN APPROACH TO A RARE HEART ANOMALY: A CASE-BASED REVIEW

Anti-Aging Eastern Europe
Dextrocardia with situs inversus, often called mirror dextrocardia, is an uncommon congenital heart defect where the heart’s apex points to the right side. The success of percutaneous coronary intervention (PCI) may contribute to its impact on individual
Darkhan Suigenbayev, Issabek Kerimkulov, Akerke Auanassova, Zhanibek Orazaly, Galiya Assanova   +4 more
doaj   +1 more source

Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This study aims to identify the imaging findings specifically for thoracic anomalies in 1200 Micro‐CT cases, independent of whether the abnormality contributed to the main diagnosis or cause of death. Method We analyzed 1200 Micro‐CT scans in an unselected, consecutive cohort between 2017 and 2024 to identify thoracic anomalies ...
Ian C. Simcock, Audrey Lamouroux, Susan C. Shelmerdine, J. Ciaran Hutchinson, Neil J. Sebire, Owen J. Arthurs   +5 more
wiley   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Transcatheter Aortic Valve Replacement in Dextrocardia With Situs Inversus

JACC: Case Reports, 2020
Transcatheter aortic valve replacement is a validated therapeutic option for severe symptomatic aortic stenosis. Dextrocardia with total situs inversus is a rare heart condition (1 in 12,000).
Gangadhar Rao Malasana, MBBS, Magdalena Zeglin, MD, Russell McElveen, DO   +2 more
doaj   +1 more source

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1719-1724, July 2026.
ABSTRACT Carpenter syndrome type 2 (CRPT2) is a rare autosomal recessive disease mainly characterized by craniosynostosis and polysyndactyly. CRPT2 is the rarer subtype of Carpenter syndrome (CRPTS) and is caused by biallelic variants in the multiple epidermal growth factor‐like domains 8 gene (MEGF8).
Kiana Rashidi, Bhavi P. Modi, Phillip A. Richmond, Massimo Mangino, Loryn Byres, Cassie McDonald, Joshua Dalmann, Simran Samra, Kate L. Del Bel, Anna Lehman, Jessica L. Zambonin, Stuart E. Turvey   +11 more
wiley   +1 more source