Osler-Rendu-Weber Disease

Brain & Nerve

Eye & Vision

+10

Contributed byLester Fahrner, MD+1 moreSep 15, 2021

The topic Osler-Rendu-Weber Disease you are seeking is a synonym, or alternative name, or is closely related to the medical condition Hereditary Hemorrhagic Telangiectasia.

Quick Summary:

Hereditary Hemorrhagic Telangiectasia (HHT) is a genetic disorder involving the blood vessels that can cause excessive bleeding, due to the formation of abnormal blood vessels called arteriovenous malformations (AVMs) in several areas of the body. It is also known as Osler-Weber-Rendu Syndrome
The AVMs can form anywhere in the body, including in the brain, lungs, liver, or intestines. When it forms on skin, it is termed telangiectasias. These malformations can result in a wide variety of signs and symptoms, such as nosebleeds, blood in urine, internal bleeding, and severe anemia, which can be life-threatening
Hereditary Hemorrhagic Telangiectasia is typically an incurable disorder, and the treatment provided is symptomatic and supportive, which may include medications and surgery, based on the healthcare provider’s assessment. The outcomes vary from one individual to another, and depends on the severity (extent of involvement of the various body organs)

Please find comprehensive information on Hereditary Hemorrhagic Telangiectasia regarding definition, distribution, risk factors, causes, signs & symptoms, diagnosis, complications, treatment, prevention, prognosis, and additional useful information HERE.

On the Article

Approved by

Krish Tangella MD, MBA

Pathology, Medical Editorial Board, DoveMed Team

Reviewed by

Lester Fahrner, MD

Chief Medical Officer, DoveMed Team

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