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You may have an increased risk for conduction disorders because of your age, family history and genetics, medical conditions, medicines, race or ethnicity, or sex. These factors can differ by the type of conduction disorder you have.

Signs and symptoms of RDS usually happen at birth or within the first few hours that follow. Depending on the severity of a newborn's RDS, he or she may develop bronchopulmonary dysplasia or other medical problems, such as bleeding in the brain, kidney failure, or lung complications.

The types of angina are stable, unstable, microvascular, and variant. The types vary based on their severity or cause.

Many people who have conduction disorders, such as first-degree AV block, may have no obvious signs or symptoms. Others may have signs and symptoms that occur in specific situations, such as when you experience physical or emotional stress or when you sleep. Conduction disorders can lead to life-threatening arrhythmias if undiagnosed or untreated.

Signs and symptoms of DIC depend on whether the condition is acute or chronic. Acute DIC is more severe and develops quickly over hours or days. Chronic DIC happens more slowly and sometimes has no signs or symptoms. Complications from DIC can occur from both the clotting that happens in the early stages of the condition and from bleeding in the later stages. Serious complications include organ damage and hemorrhage.

The signs, symptoms, and complications of vasculitis vary depending on which type of vasculitis you have, the organs involved, and the severity of the condition. Some people may have few signs and symptoms. Other people may become very sick.

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.

Su riesgo de desarrollar trastornos hemorrágicos puede aumentar por la edad, el historial familiar y genético, otras afecciones médicas y medicinas, y el sexo.

Los signos, síntomas y complicaciones pueden variar según el tipo de trastorno hemorrágico, su causa y si el trastorno es leve o más grave. Los signos y síntomas pueden ser obvios poco después del nacimiento de un niño o pueden no aparecer hasta la edad adulta. Las personas que tienen un trastorno hemorrágico leve pueden no tener ningún signo o síntoma hasta que se lesionen o tengan un procedimiento médico.