Hypoplastic right heart syndrome

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Hypoplastic right heart syndrome
Synonyms HRHS
Pronounce
Specialty Cardiology, Pediatric cardiology
Symptoms Cyanosis, dyspnea, fatigue, poor feeding
Complications Heart failure, arrhythmias, pulmonary hypertension
Onset Congenital
Duration Lifelong
Types
Causes Congenital heart defect
Risks Genetic factors, maternal diabetes, maternal smoking
Diagnosis Echocardiogram, fetal ultrasound, cardiac MRI
Differential diagnosis Tetralogy of Fallot, tricuspid atresia, pulmonary atresia
Prevention
Treatment Surgery, medication, heart transplant
Medication Prostaglandin E1, diuretics, ACE inhibitors
Prognosis Variable, depends on severity and treatment
Frequency Rare
Deaths


Hypoplastic Right Heart Syndrome

Hypoplastic right heart syndrome (HRHS) is a rare congenital heart defect in which the right side of the heart is underdeveloped. It affects the right ventricle and the valves that control the flow of blood between the right atrium and the right ventricle (the tricuspid and pulmonary valves).

Causes[edit]

The exact cause of HRHS is unknown, but it is believed to occur during the first 8 weeks of fetal development. Some research suggests that a combination of genes and environmental factors may play a role. Certain conditions, such as diabetes in the mother, have been associated with a higher risk of having a child with HRHS.

Symptoms[edit]

Symptoms of HRHS can vary greatly depending on the severity of the condition. They may include rapid breathing, difficulty feeding, lethargy, and a bluish color to the skin, lips, and nails (known as cyanosis) due to low oxygen levels in the blood. In severe cases, HRHS can lead to heart failure.

Diagnosis[edit]

HRHS is typically diagnosed through an echocardiogram, which uses sound waves to create a detailed image of the heart's structure and function. Other tests, such as a cardiac catheterization, may be used to confirm the diagnosis and assess the severity of the condition.

Treatment[edit]

Treatment for HRHS typically involves multiple surgeries to re-route the blood flow around the underdeveloped right side of the heart. The first surgery, known as the Norwood procedure, is usually performed within the first week of life. Subsequent surgeries, including the Glenn procedure and the Fontan procedure, are performed over the next several years.

Prognosis[edit]

With early diagnosis and treatment, many children with HRHS can lead relatively normal lives. However, they will require lifelong medical care and may have limitations on their physical activity.

See also[edit]






Cardiovascular disease A-Z

Most common cardiac diseases

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