Results 41 to 50 of about 8,062 (214)
An Evolutionary Hypothesis of Binary Opposition in Functional Incompatibility about Habenular Asymmetry in Vertebrates [PDF]
, 2017 Many vertebrates have asymmetrical circuits in the nervous system. There are two types of circuit asymmetry. Asymmetrical circuits in sensory and/or motor systems are usually related to lateralized behaviors.
Agetsuma +63 more
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Creating a Fontan fenestration in a child with dextrocardia and interrupted inferior vena cava [PDF]
, 2016 Plastic bronchitis is a rare life-threatening complication of the Fontan operation. Transcatheter Fontan fenestration can ameliorate symptoms by decompressing elevated venous pressures.
Breinholt, John P. +1 more
core +3 more sources
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 +2 more
doaj +1 more source
CARDIAC STENTING IN DEXTROCARDIA- AN APPROACH TO A RARE HEART ANOMALY: A CASE-BASED REVIEW
Anti-Aging Eastern EuropeDextrocardia 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 +4 more
doaj +1 more source
Cor triatriatum sinister with situs inversus totalis in an infant. [PDF]
, 2012 Cor triatriatum sinister is a rare congenital cardiac malformation characterized by a membrane in the left atrium which separates the left atrium into the proximal and distal chambers.Association of cor triatriatum is extremely rare with situs inversus
Gadekar, A. +3 more
core +1 more source
American Journal of Medical Genetics Part A, EarlyView.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
Assessment of copy number variations in 120 patients with Poland syndrome [PDF]
, 2016 Poland Syndrome (PS) is a rare congenital disorder presenting with agenesis/hypoplasia of the pectoralis major muscle variably associated with thoracic and/or upper limb anomalies.
Aldamaria Puliti +17 more
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Catheterization and Cardiovascular Interventions, EarlyView.ABSTRACT Background Mitral regurgitation (MR) is the valent type of valvular heart disease, caused by primary leaflet lesions or annular dilatation secondary to left ventricular dysfunction. It can lead to a series of complications such as volume overload, exacerbated pulmonary congestion, and heart failure, significantly impacting patient prognosis ...
Juelian Li +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 +2 more
doaj +1 more source
Cantrell Syndrome. Case report of an adult [PDF]
, 2000 Cantrell syndrome is characterized by defects that involve the diaphragm, abdominal wall, pericardium, heart, and lower region of the sternum. It is a rare entity, usually diagnosed at birth and accompanied by high mortality due to the complexity and ...
Falcão, João Luiz Alencar Araripe +4 more
core +5 more sources