Results 31 to 40 of about 2,596,890 (367)
BMC Pregnancy and Childbirth, 2020 Background Fetal double aortic arch (DAA) malformation is a rare congenital heart disease with few reported cases in the literature. We aimed to investigate the characteristics of prenatal ultrasound and postnatal computed tomography angiography (CTA) of
Qiao Guo +11 more
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Aortic Arch Anomalies and Pulmonary Artery Anomalies : Echocardiographic Evaluation
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2020 Congenital variants and anomalies of the aortic arch are important to recognize as they may be associated with vascular rings, congenital heart disease, and chromosomal abnormalities, and can have important implications for prognosis and management.
Prashant Mahawar
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Ultrasound in Obstetrics and Gynecology, 2020 Vascular rings are congenital aortic arch anomalies that compress the trachea and esophagus, causing symptoms related to these two structures. One of the common types of vascular ring is formed by a right aortic arch, aberrant left subclavian artery and ...
B. Ma, Lin Wu, Wei Zhang
semanticscholar +1 more source
DOUBLE AORTIC ARCH - A CASE REPORT912
Pakistan Armed Forces Medical Journal, 2020 Double Aortic Arch is a rare congenital cardiovascular anomaly. Its first successful surgery was performed by Robert Gross in 1945 at Children Hospital Boston, USA. It accounts for 0.4 to 1% of all congenital cardiac defects.
Syed Shahid Nafees +3 more
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Trends in vascular ring surgery [PDF]
The Journal of Thoracic and Cardiovascular Surgery, 2005 We sought to review our experience with infants and children with anatomically complete vascular rings (ie, double aortic arch and right aortic arch with left ligamentum) and define perioperative trends in diagnostic imaging, operative techniques, and clinical outcomes.From 1946 through 2003, 209 patients (113 with double aortic arch and 96 with right ...
Cynthia K. Rigsby +3 more
openaire +3 more sources
Veterinární Medicína, 2017 The paper describes a double symmetrical aortic arch in a dog trapping the oesophagus. Thoracotomy was performed in the fourth inter-costal space under general, isoflurane-maintained, anaesthesia.
P. Skrzypczak +3 more
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Romanian Journal of Cardiology, 2023 Pulmonary agenesis is a rare malformation associated with congenital heart disease and may lead to a life-threatening condition and death without pre-planned surgical and medical support.
Delikatnyi Maksym +5 more
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22q11.2 microduplication syndrome with associated esophageal atresia/tracheo-esophageal fistula and vascular ring. [PDF]
Clin Case Rep, 2017 This case report describes a patient with a 22q11.2 duplication. His features, which include VACTERL association with an esophageal atresia/tracheo‐esophageal fistula and a vascular ring, expand the previously described phenotype for this duplication.
Nguyen LT +7 more
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Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia [PDF]
, 2015 Deletion of exon 9 from Cullin‐3 (CUL3, residues 403–459: CUL3Δ403–459) causes pseudohypoaldosteronism type IIE (PHA2E), a severe form of familial hyperkalaemia and hypertension (FHHt).
Al Maskari, Raya S. +14 more
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Management of double aortic arch in children
Iranian Journal of Pediatric Surgery, 2016 Introduction: Double aortic arch (DAA) is a rare congenital malformation. Strategies for diagnosis and treatment are different. Reports of thoracoscopic treatment of DAA are rare.
Samia Belhassen +8 more
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