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  2. Tetralogy of Fallot - Wikipedia

    en.wikipedia.org/wiki/Tetralogy_of_Fallot

    Tetralogy of Fallot (TOF), formerly known as Steno-Fallot tetralogy, [9] is a congenital heart defect characterized by four specific cardiac defects. [4] Classically, the four defects are: [ 4 ] pulmonary stenosis , which is narrowing of the exit from the right ventricle;

  3. Blalock–Thomas–Taussig shunt - Wikipedia

    en.wikipedia.org/wiki/Blalock–Thomas–Taussig...

    The Blalock–Thomas–Taussig shunt (BTT shunt), [1] previously known as the Blalock–Taussig Shunt (BT shunt), [2] is a surgical procedure used to increase blood flow to the lungs in some forms of congenital heart disease [3] such as pulmonary atresia and tetralogy of Fallot, which are common causes of blue baby syndrome. [3]

  4. Trilogy of Fallot - Wikipedia

    en.wikipedia.org/wiki/Trilogy_of_Fallot

    Trilogy of Fallot is a combination of three congenital heart defects: pulmonary stenosis, right ventricular hypertrophy, and an atrial septal defect. [1]The first two of these are also found in the more common tetralogy of Fallot.

  5. Wikipedia:Osmosis/Tetralogy of Fallot - Wikipedia

    en.wikipedia.org/.../Tetralogy_of_Fallot

    Tetralogy of Fallot is actually the most common cause of cyanotic congenital heart defects, accounting for about 50-70%, as well as about 10% of all congenital heart defects in general. Now, it’s not quite clear why some babies develop TOF but it is associated with chromosome 22 deletions and DiGeorge syndrome.

  6. Eileen Saxon - Wikipedia

    en.wikipedia.org/wiki/Eileen_Saxon

    She had a condition called Tetralogy of Fallot, one of the primary congenital defects that lead to blue baby syndrome. In this condition, defects in the great vessels and wall of the heart lead to a chronic lack of oxygen in the blood. In Eileen's case, this made her lips and fingers turn blue, with the rest of her skin having a very faint blue ...

  7. Absent pulmonary valve syndrome - Wikipedia

    en.wikipedia.org/wiki/Absent_pulmonary_valve...

    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]

  8. Smith–Martin–Dodd syndrome - Wikipedia

    en.wikipedia.org/wiki/Smith–Martin–Dodd_syndrome

    It is characterized by small eyes, a diaphragmatic hernia, and Tetralogy of Fallot, a congenital heart defect. [2] [3] The only known case is of a 9-year-old boy with several congenital anomalies including a diaphragmatic hernia, microphthalmia, and Tetralogy of Fallot. It was found that the boy had a reciprocal translocation t(1;15)(q41;q21.2 ...

  9. Cyanotic heart defect - Wikipedia

    en.wikipedia.org/wiki/Cyanotic_heart_defect

    Tetralogy of Fallot (ToF) Total anomalous pulmonary venous connection; Hypoplastic left heart syndrome (HLHS) Transposition of the great arteries (d-TGA) Truncus arteriosus (Persistent) Tricuspid atresia; Interrupted aortic arch; Pulmonary atresia (PA) Pulmonary stenosis (critical) Eisenmenger syndrome (reversal of shunt due to pulmonary ...