Lifelong condition; management focuses on addressing specific symptoms and needs
Marfan syndrome is a genetic disorder affecting connective tissues, leading to skeletal, cardiovascular, and ocular abnormalities. Treatment focuses on managing symptoms, often involving a multidisciplinary approach. Regular monitoring is essential for early detection and intervention. Lifestyle modifications and medications may be recommended to address specific aspects of the syndrome.
Genetic connective tissue disorder affecting the heart, eyes, and skeleton
Tall stature, long limbs, heart and eye complications
Clinical evaluation, genetic testing
Variable, depends on the severity of symptoms
Cardiovascular complications, complications affecting multiple systems
Genetic mutation
Symptomatic treatment, monitoring of complications
Symptomatic treatment, monitoring of complications
Genetic connective tissue disorder
Monitoring, management of symptoms, sometimes surgery
Remember, the information provided here is intended for general knowledge purposes and may not apply to every individual case. To ensure you have accurate information relevant to your specific situation, always consult with a healthcare professional.
Share: