Results 61 to 70 of about 6,363 (156)
Journal of the Saudi Heart Association, 2017 Clinical research. Presentation Type: Oral Presentation Introduction: Dextrocardia is the right-sided positioning of the human heart during embryological development. It may be isolated or associated with visceral dextroposition or malformations.
Naif Alghasab +13 more
doaj +1 more source
Situs inversus totalis with azoospermia in a patient presenting with liver abscess [PDF]
Journal of Clinical and Scientific Research, 2014 Situs inversus with dextrocardia is a rare congenital anomaly. Azoospermia and situs inversus may be encountered in ciliary dyskinesia syndromes.
P. Mohan Rao +4 more
doaj +1 more source
A modality‐agnostic coronary artery habitat model for cardiac sparing in radiotherapy
Medical Physics, Volume 53, Issue 8, August 2026.Abstract Background Emerging evidence suggests that the risk of cardiotoxicity increases with increased radiation dose to coronary arteries (CAs). However, robust tools to evaluate this increased burden for cancer patients are not available due to current limitations in imaging for radiotherapy treatment planning.
Chase Ruff +6 more
wiley +1 more source
Pediatric Pulmonology, Volume 61, Issue 8, August 2026.ABSTRACT Background Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder, and despite advances in next‐generation sequencing, a substantial proportion of clinically suspected pediatric cases remain without a molecular diagnosis.
Tilbe Hakçıl Öz +4 more
wiley +1 more source
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 +4 more
wiley +1 more source
BALLER-GEROLD SYNDROME ASSOCIATED WITH DEXTROCARDIA
, 2011 Baller-Gerold syndrome associated with dextrocardia: Baller-Gerold Syndrome (BGS) is a rare autosomal recessive disorder that is apparent at birth. The disorder is characterized by distinctive malformations of the skull and facial area and bones of the ...
Ceylan, A. +4 more
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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 +11 more
wiley +1 more source
Kartagener Syndrome: A Rare Genetic Disorder
Journal of Nepal Medical Association, 2009 Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchiectasis and situs inversus with dextrocardia. It is the subset of disorder called primary ciliary dyskinesia in which the cilia have abnormal structure ...
Kunjan Shakya
doaj +1 more source
Essential embryology for the Canadian pathologists’ assistant
Anatomical Sciences Education, Volume 19, Issue 7, Page 1134-1156, July 2026.Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci +4 more
wiley +1 more source
Mirror Image Dextrocardia with Severe Rheumatic Mitral Stenosis Undergone Successful Percutaneous Transvenous Commissurotomy: The First Case in East Africa [PDF]
Kefelegn Dejene Tadesse,1 Yidnekachew Asrat Birhan2 1Cardiology Department, Cardiac Center of Ethiopia, Addis Ababa, Ethiopia; 2Internal Medicine Department, Addis Ababa University, Addis Ababa, EthiopiaCorrespondence: Kefelegn Dejene Tadesse, Email ...
Tadesse KD, Birhan YA
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