Raghib syndrome
Raghib Syndrome
Raghib syndrome (/rɑːɡiːb/; from Arabic راغب, meaning "desiring") is a rare congenital disorder characterized by the combination of congenital heart disease and abnormalities of the superior vena cava and left atrium.
Etymology
The syndrome is named after Dr. Mohammed Raghib, who first described the condition in 1965. The term "Raghib" is of Arabic origin, meaning "desiring".
Symptoms and Signs
Patients with Raghib syndrome typically present with symptoms of congestive heart failure, including shortness of breath, fatigue, and edema. Other signs may include cyanosis, murmur, and arrhythmia.
Diagnosis
Diagnosis of Raghib syndrome is typically made through echocardiography, which can reveal the characteristic heart abnormalities. Other diagnostic tests may include cardiac catheterization and magnetic resonance imaging (MRI).
Treatment
Treatment for Raghib syndrome typically involves surgery to correct the heart defects. Medications may also be used to manage symptoms of heart failure.
Prognosis
The prognosis for individuals with Raghib syndrome varies depending on the severity of the heart defects and the individual's overall health. With appropriate treatment, many individuals with Raghib syndrome can lead normal lives.
See Also
External links
- Medical encyclopedia article on Raghib syndrome
- Wikipedia's article - Raghib syndrome
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