Final answer:
Osler-Rendu-Parkes Weber syndrome (Hereditary Hemorrhagic Telangiectasia) is a genetic disorder characterized by the formation of dilated, twisted blood vessels known as telangiectasias. It affects various organs in the body and presents common symptoms such as nosebleeds, skin telangiectasias, and arteriovenous malformations (AVMs).
Step-by-step explanation:
Osler-Rendu-Parkes Weber syndrome, also known as Hereditary Hemorrhagic Telangiectasia (HHT), is a genetic disorder that affects blood vessels throughout the body.
It is characterized by the formation of dilated, twisted blood vessels called telangiectasias, which can occur in various organs such as the skin, mucous membranes, and internal organs.
Common symptoms include recurrent nosebleeds, telangiectasias on the skin, and arteriovenous malformations (AVMs), which are abnormal connections between arteries and veins.
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