Loeys-Dietz syndrome

From WikiMD.org
Jump to navigation Jump to search

Loeys-Dietz syndrome

Loeys-Dietz syndrome (pronounced: loys deetz sin-drohm) is a rare genetic disorder that affects the body's connective tissue. It is named after the two doctors, Dr. Bart Loeys and Dr. Hal Dietz, who first identified the condition in 2005.

Etymology

The syndrome is named after Dr. Bart Loeys and Dr. Hal Dietz, who first described the condition in 2005. The term "syndrome" is derived from the Greek word "syndromē", which means "concurrence of symptoms, concourse of people".

Definition

Loeys-Dietz syndrome is a genetic disorder characterized by the enlargement of the aorta, the main blood vessel that carries blood from the heart to the rest of the body. This can lead to an aortic aneurysm, a bulge in the wall of the aorta that can rupture and cause life-threatening bleeding.

Symptoms

Symptoms of Loeys-Dietz syndrome can vary greatly from person to person, but may include:

Diagnosis

Diagnosis of Loeys-Dietz syndrome is typically made through a combination of physical examination, medical history, and genetic testing. Imaging tests such as echocardiogram, computed tomography (CT) scan, or magnetic resonance imaging (MRI) may also be used to identify abnormalities in the aorta or other arteries.

Treatment

Treatment for Loeys-Dietz syndrome typically involves managing symptoms and preventing complications. This may include medications to lower blood pressure, surgery to repair or replace the aorta, and regular monitoring of the heart and blood vessels.

Related Terms

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski