Searching for Telangiectasia Support information? Find all needed info by using official links provided below.
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https://rarediseases.info.nih.gov/diseases/10690/macular-telangiectasia-type-2
May 03, 2018 · Macular telangiectasia (MacTel) type 2 is an eye disease affecting the macula that causes loss of central vision. MacTel develops when there are problems with the tiny blood vessels (capillaries) around the fovea, an area in the center of the macula where eyesight is the sharpest.In MacTel type 2, the capillaries around the fovea widen (become dilated) and leak.
https://www.healthline.com/health/telangiectasia
Nov 29, 2017 · Telangiectasia is a condition in which widened venules (tiny blood vessels) cause threadlike red lines or patterns on the skin. These patterns, or telangiectases, form …
Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu Syndrome, is an inherited disease that leads to malformed blood vessels in multiple organs of the body and typically begins with nosebleeds during childhood. HHT can result in serious health problems if not promptly diagnosed and treated.
https://www.stjude.org/disease/ataxia-telangiectasia.html
Because ataxia-telangiectasia is a complex condition, it is very important that parents seek out an experienced doctor for their child. How is ataxia-telangiectasia diagnosed? A doctor may suspect ataxia-telangiectasia based on signs and symptoms of the condition. Several lab tests can be used to support a clinical diagnosis of ataxia ...
https://ghr.nlm.nih.gov/condition/hereditary-hemorrhagic-telangiectasia
Oct 29, 2019 · Hereditary hemorrhagic telangiectasia is a disorder that results in the development of multiple abnormalities in the blood vessels.. In the circulatory system, blood carrying oxygen from the lungs is normally pumped by the heart into the arteries at high pressure. The pressure allows the blood to make its way through the arteries to the smaller vessels (arterioles and capillaries) that supply ...
https://en.wikipedia.org/wiki/Ataxia_telangiectasia
Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both …Specialty: Neurology, medical genetics
https://ghr.nlm.nih.gov/condition/ataxia-telangiectasia
Oct 15, 2019 · Ataxia-telangiectasia is a rare inherited disorder that affects the nervous system, immune system, and other body systems. This disorder is characterized by progressive difficulty with coordinating movements (ataxia) beginning in early childhood, usually before age 5.
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