Search Media Items

Marfan syndrome is a genetic condition caused by a mutation, or change, in one of your genes, called the fibrillin-1 (FBN1) gene. The FBN1 gene makes fibrillin-1, which is a protein that forms elastic fibers within connective tissue. Fibrillin-1 also affects levels of another protein that helps control how you grow.

If you have a known family history of Marfan syndrome or physical features of the condition, your doctor may recommend screening to find the condition early. Relatives of people who have Marfan syndrome may also want to have genetic screening. There is no way to prevent Marfan syndrome.

Una alimentación saludable para el corazón incluye vegetales, frutas, granos enteros, productos lácteos sin grasa o bajos en grasa, pescado, carnes magras (con poca grasa), pollo y otras aves, huevos, nueces, semillas, productos de soya, legumbres y aceites vegetales (excepto los aceites de coco y de palma). Además, limita el sodio, las grasas saturadas y grasas trans, los azúcares agregados y el alcohol.

Treatments for carotid artery disease may include heart-healthy lifestyle changes, medicines, and medical procedures such as carotid endarterectomy and carotid artery angioplasty and stenting.

Factors that increase your risk for high blood pressure include unhealthy lifestyle habits such as eating too much sodium, drinking too much alcohol, and being physically inactive. Other risk factors include age, family history and genetics, race and ethnicity, and sex.

Age, race, gender, certain medical conditions—high blood pressure, diabetes, brain aneurysms, and heart diseases—smoking, and family history can raise your risk for a stroke.

Signs, symptoms, and complications will vary based on the type of congenital heart defect that you or your child have, and may be different for newborns and adults.

La enfermedad coronaria es una enfermedad en la cual una sustancia cerosa llamada placa se acumula dentro de las arterias coronarias a través de muchos años. Estas arterias suministran sangre rica en oxígeno al músculo cardíaco.

At first, COPD may cause no symptoms or only mild symptoms. As the disease worsens, common signs and symptoms include an ongoing cough (with or without mucus), shortness of breath, wheezing or whistling when breathing, and chest tightness.

Congenital heart defects happen because the heart does not develop normally while the baby is growing in the womb. Doctors often do not know why congenital heart defects occur. Researchers do know that genetics can sometimes play a role.