Results 41 to 50 of about 822 (143)
Prenatal Diagnosis of Horseshoe Lung: A Report of Three Cases and Review of the Literature
ABSTRACT Objective Horseshoe lung is a rare congenital malformation in which the lungs are fused by a parenchymal isthmus. The current literature is very limited regarding cases of prenatal diagnosis and their outcome. Method We retrospectively examined three cases of fetuses with horseshoe lung diagnosed antenatally in our center from 2015 to 2024 ...
Benjamin Birene +6 more
wiley +1 more source
Left Bundle Branch Pacing in a Patient With Dextroposed Heart: A Case Report
ABSTRACT The Right Ventricular (RV) apex has been the standard site for pacing in symptomatic bradyarrhythmias, but chronic RV pacing can cause adverse effects such as atrial arrhythmias and left ventricular dysfunction. Physiological pacing, including His bundle and left bundle pacing, offers alternatives with fewer complications. We present a 66‐year‐
Dilip Kumar +7 more
wiley +1 more source
Clinical and Surgical Perspectives on Isolated Thoracic Ectopia Cordis: A Rare Case Report
Ectopia cordis is an exceptionally uncommon congenital condition where the heart develops outside its normal position due to incomplete closure of the ventral chest wall during embryogenesis. The anomaly may occur in isolation or with other structural defects, often resulting in a poor prognosis despite advancements in medical and surgical care.
Syed Mohsin Raza Bukhari +9 more
wiley +1 more source
Pulmonary valve atresia (PVA) is a fatal pediatric cardiac condition and commonly associated with other anomalies such as double outlet right ventricle (DORV).
Mohammed Rasool Hussein +2 more
doaj +1 more source
Congenital Corrected Transposition of Great Arteries in Adults with Varied Presentation
Congenital corrected transportation of great arteries (ccTGA) is a rare congenital heart disease, accounting for < 1% of congenital heart diseases. It remains undiagnosed until adulthood, in the absence of associated congenital anomalies.
Akshay Narendra Kotasthane +3 more
doaj +1 more source
Clinical presentation and short‐term outcomes of dogs ≥15 kg with extrahepatic portosystemic shunts
Abstract Objective To describe demographics, clinical presentation, shunt anatomy, clinical progression, and complications in large dogs ≥15 kg with single extrahepatic portosystemic shunts (EHPSS) treated with or without surgery. Study Design Multicenter retrospective (10 university hospitals, one private referral institution). Animals Dogs ≥15 kg (n =
Kate Spies +16 more
wiley +1 more source
A Case Report of Dextrocardia with Situs Inversus: A Rare Condition and Its Clinical Importance
Situs inversus totalis (SIT) is a rare medical condition characterized by a complete mirror‐image reversal of the normal positioning of the internal organs. Aristotle initially described situs inversus in animals, while Fabricius first characterized it in humans.
Girma Deshimo +5 more
wiley +1 more source
Patient with congenital heart malformation and infective endocarditis
We present the case of a 17 year-old-man, with no remarkable past medical history, who had a one month history of worsening functional class, fatigability and dyspnea, in addition to fever and systemic inflammatory response syndrome (SIRS); a de-novo ...
Ramírez Ortiz, Zoraida +2 more
doaj
Tetralogy of Fallot (TOF) is a significant cause of cyanotic congenital heart disease (CHD) encountered in childhood with few cases manifesting in adulthood. It has four classical features (ventricular septal defect, overriding of aorta, hypertrophy of right ventricular hypertrophy, and right ventricular outflow tract obstruction), but the clinical ...
Abhishek Dwivedi +5 more
wiley +1 more source
Paciente con malformación cardíaca congénita y endocarditis infecciosa
Se presenta el caso de un hombre de 17 años, sin antecedentes de importancia, quien consultó por un mes de evolución de deterioro de su clase funcional, fatigabilidad y disnea, además de fiebre y síndrome de respuesta inflamatoria sistémica (SIRS) en ...
Zoraida Ramírez Ortiz +2 more
doaj

