Can Tetralogy of Fallot be cured?

Written by Yan Xin Liang
Pediatrics
Updated on May 19, 2025
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Tetralogy of Fallot consists of four types of cardiac malformations: first, a ventricular septal defect; second, right ventricular outflow tract obstruction; third, an overriding aorta; and fourth, right ventricular hypertrophy. The main treatment for this condition is surgical repair. In recent years, there have been continual advancements in surgical procedures. Many children undergo a definitive one-stage surgery in early childhood, which can completely cure the condition. Thus, if the symptoms are mild, a definitive surgery can be performed in one stage. If the symptoms are more severe, a palliative shunt surgery may be performed first, followed by the definitive surgery when the general condition improves, and it can still be cured.

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Written by Hu Qi Feng
Pediatrics
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Tetralogy of Fallot Clinical Characteristics

Tetralogy of Fallot is the most common cyanotic congenital heart disease in infancy, accounting for about 12% of all congenital heart diseases. It is caused by malformations of four heart structures: 1. right ventricular outflow tract obstruction; 2. ventricular septal defect; 3. overriding aorta; 4. right ventricular hypertrophy. Its clinical manifestations may include cyanosis, squatting symptoms, clubbed fingers, and paroxysmal hypoxia attacks. Physical examinations generally show delayed development, a prominent precordial area, and at the second to fourth rib interspace along the left sternal margin, a grade 2 to 3 rough systolic murmur can be heard.

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Written by Yan Xin Liang
Pediatrics
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Is tetralogy of Fallot a chromosomal problem?

Tetralogy of Fallot is the most common cyanotic congenital heart disease in childhood, consisting of four defects: ventricular septal defect, obstruction of the right ventricular outflow tract, overriding aorta, and right ventricular hypertrophy. It is a type of congenital heart disease, which generally stems from abnormal cardiovascular development during fetal life, resulting in cardiovascular malformations not controlled by chromosomes. The malformation of the cardiovascular system is mainly caused by genetic factors, environmental factors, and their interactions. The exact cause of this congenital heart disease has not been fully identified yet, indicating that it is not a chromosomal disease but a result of cardiovascular developmental abnormalities during fetal life.

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Written by Hu Qi Feng
Pediatrics
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Tetralogy of Fallot Common Symptoms

The clinical manifestations of Tetralogy of Fallot include, firstly, cyanosis as the primary clinical symptom. The degree and onset of cyanosis are related to the severity of pulmonary stenosis, and it often appears in areas with abundant capillaries such as lips, fingers, toes, nail beds, and bulbar conjunctiva. Secondly, squatting symptoms are common among children; they often spontaneously squat for a while during walking or playing. Squatting, with the legs bent, reduces the venous return and thus decreases the load on the heart, temporarily relieving symptoms of hypoxia by reducing the right-to-left shunt. Thirdly, clubbing occurs due to long-term hypoxic conditions, which can cause capillary dilation and proliferation in the fingers and toes, and the local soft tissues and bones also grow and enlarge; fourthly, paroxysmal hypoxic attacks, which are most common in infants, can be triggered by breastfeeding, crying, emotional excitement, or anemia. These attacks suddenly occur and can lead to severe symptoms including difficulty breathing, fainting, convulsions, and even death.

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Written by Du Rui Xia
Obstetrics
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Can tetralogy of Fallot be detected by prenatal screening?

During prenatal check-ups for fetuses diagnosed with Tetralogy of Fallot, the condition can be detected. A four-dimensional color Doppler ultrasound can be performed in the mid-pregnancy stage, allowing observation of the fetus's development, such as the brain, kidneys, skeleton, and heart. Therefore, using four-dimensional color Doppler ultrasound checks can identify congenital heart diseases. When Tetralogy of Fallot is diagnosed, deciding whether to continue with the pregnancy or terminate it is a major concern for the pregnant woman. Cardiac malformations in the fetus can also be surgically treated after birth.

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Written by Yan Xin Liang
Pediatrics
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Is Tetralogy of Fallot hereditary?

Tetralogy of Fallot is a common cyanotic congenital heart disease in children, accounting for about ten percent of congenital heart diseases. It primarily consists of four abnormalities: ventricular septal defect, right ventricular outflow tract obstruction, overriding aorta, and left ventricular hypertrophy. Congenital heart disease is not a hereditary disease; it is not controlled by genes, mainly due to abnormal development of the heart and blood vessels during fetal development, leading to cardiovascular malformations. Thus, this disease is not hereditary.