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Tetralogy of Fallot; Other names: Fallot’s syndrome, Fallot’s tetrad, Steno–Fallot tetralogy [1] Diagram of a healthy heart and one with tetralogy of Fallot: Specialty: Cardiac surgery, pediatrics: Symptoms: Episodes of bluish color to the skin, difficulty breathing, heart murmur, finger clubbing [2] Complications
Tetralogy of Fallot: pulmonary stenosis, ventricular septal defect, right ventricular hypertrophy, overriding aorta: Tetralogy of Fallot Ménière's disease: vertigo, tinnitus, fluctuating low frequency hearing loss, aural fullness: Ménière's disease zoonotic tetrad: scrub typhus, chiggers, rodents and birds, scrub vegetation
Neonatal diabetes is classified into three subtypes: permanent, transient, and syndromic; each with distinct genetic causes and symptoms. [5] Syndromic neonatal diabetes is the term for diabetes as just one component of any of several complex syndromes that affect neonates, including IPEX syndrome, Wolcott-Rallison syndrome, and Wolfram ...
A diagnosis of TOF is usually made with echocardiography, which can even be done prenatally. Most patients with tetralogy of Fallot will have cardiac repair surgery in the first year of life, where the ventricular septal defect is closed with a patch, and the right ventricular outflow tract is enlarged.
Cœur en sabot (French for "clog-shaped heart" or "boot-shaped heart" [1]) is a radiological sign seen most commonly in patients with tetralogy of Fallot, [2] a cyanotic congenital heart disease. It is a radiological term to describe the following findings in the x-ray: [ citation needed ]
2.1 Differential diagnosis. 3 Treatment. 4 History. 5 References. Toggle the table of contents. Warsaw breakage syndrome. 1 language. ... Tetralogy of Fallot ...
Higher amounts than this were linked to a higher risk of having children with septal defects and/or obstruction of the left ventricular outflow tract. [42] Other risk factors include maternal obesity, diabetes, rubella, indomethacin tocolysis, phenylketonuria, or elderly age. [43] [9]
The most typical form of APVS is a tetralogy of Fallot variant, [4] however, case studies have linked APVS to several different congenital cardiac syndromes, such as agenesis of ductus arteriosus, [5] persistent ductus arteriosus, [6] atrioventricular septal defect, [7] pulmonary branching abnormalities, [8] [9] transposition of the great arteries, [10] and type B interrupted aortic arch. [11]
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