Results 71 to 80 of about 13,117 (209)
Combining pulse‐field ablation with a 3D mapping system allowed a safe, zero‐fluoroscopy atrial fibrillation ablation procedure in situs inversus, overcoming catheter loss of catheter orientation due to mirror‐image anatomy.
Tadashi Hoshiyama +3 more
wiley +1 more source
Background Situs inversus is a rare congenital condition that is currently classified into two types: complete situs inversus (situs inversus totalis, SIT) and partial situs inversus (situs inversus partialis, SIP).
Yuki Aisu +5 more
doaj +1 more source
Fetal heterotaxy with tricuspid atresia, pulmonary atresia, and isomerism of the right atrial appendages at 22 weeks. [PDF]
We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex ...
Richardson, Randy R +3 more
core +2 more sources
ABSTRACT Primary ciliary dyskinesia (PCD) is a rare inherited disease which is characterised by progressive lung disease, chronic rhinosinusitis, repeated middle ear infections, laterality defects, and reduced fertility. An early diagnosis is critical to reduce morbidity, however diagnosis is often delayed due to the heterogeneity in clinical ...
Katharine Harman +2 more
wiley +1 more source
SITUS INVERSUS TOTALIS WITH LIVER ABCESS
A case of multiple liver abscesses in a patient with situs inversus totalis is presented. Initially the patient was treated conservatively and remained symptom free for 4 days of hospital stay. On a follow up visit after 1 week the patient had high grade
Tariq Saeed Mufti +3 more
doaj
Colecistectomia laparoscopica in situs viscerum inversus totalis: nota di tecnica [PDF]
The Authors report the case of a patient admitted in Emergency Room for biliary colic. She knew her dextrocardia. ECG and chest X-ray confirmed the dextrocardia.
Di Luna, G. +5 more
core
PICADAR: a diagnostic predictive tool for primary ciliary dyskinesia [PDF]
Symptoms of primary ciliary dyskinesia (PCD) are nonspecific and guidance on whom to refer for testing is limited. Diagnostic tests for PCD are highly specialised, requiring expensive equipment and experienced PCD scientists. This study aims to develop a
Behan, Laura +10 more
core +1 more source
ABSTRACT Background No consistent genetic etiology has been found for a group of six different conditions in humans with multiple malformations called “recurrent constellations of embryonic malformations” (RCEM). Recent studies indicate hypoxia/reoxygenation and generation Reactive Oxygen Species (ROS) as an underlying mechanism for RCEM with the ...
Aaron P. Adam +3 more
wiley +1 more source
Situs inversus and heterotaxy syndromes are rare and often complicated conditions that involve an abnormal arrangement of the thoracic and abdominal organs. Congenital heart defects and other complications are often present with these conditions. There is no corrective surgery recommended or available, other than for the specific cardiac anomalies ...
openaire +2 more sources
ABSTRACT Kartagener's Syndrome (KS), a rare autosomal recessive disorder and a subset of Primary Ciliary Dyskinesia (PCD), is characterized by chronic sinusitis, bronchiectasis, and, in approximately 50% of cases, situs inversus. This condition arises from genetic mutations that impair motile cilia function, leading to defective mucociliary clearance ...
Ibrahim Khalil +3 more
wiley +1 more source

