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- Hereditary hemorrhagic telangiectasia - Symptoms and causes
Hereditary hemorrhagic telangiectasia (tuh-lan-jee-uk-TAY-zhuh) is a condition that's passed through families, called inherited It causes atypical links between arteries and veins called arteriovenous malformations (AVMs)
- Hereditary Hemorrhagic Telangiectasia (HHT) - StatPearls - NCBI Bookshelf
Hereditary hemorrhagic telangiectasias (HHT) is an autosomal dominant bleeding disorder caused by malformed vessels The condition manifests as telangiectasias affecting the skin and mucosa and arteriovenous malformations involving organs like the lung, brain, and liver
- Hereditary hemorrhagic telangiectasia - Wikipedia
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler–Weber–Rendu disease and Osler–Weber–Rendu syndrome, is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver, and brain
- Hereditary Hemorrhagic Telangiectasia (HHT) - Johns Hopkins Medicine
Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder of the blood vessels that can occur in the brain, lungs, digestive system, skin or other organs Symptoms of hereditary hemorrhagic telangiectasia can be absent or subtle, and may not show up until adulthood
- About Hereditary Hemorrhagic Telangiectasia (HHT)
HHT is a genetic disorder in which blood vessels do not develop normally leading to bleeding that can be serious or life threatening Frequent nosebleeds are the most common sign Complication can vary widely, even among affected family members Treatment to control bleeding and prevent complications may be needed
- Hereditary Hemorrhagic Telangiectasia (HHT) - Cleveland Clinic
Hereditary hemorrhagic telangiectasia (HHT), also called Osler-Weber-Rendu syndrome, is a genetic disorder that affects blood vessel formation People with HHT develop small lesions called telangiectases, which can burst and bleed
- Hereditary hemorrhagic telangiectasia (HHT): a practical guide to . . .
Hereditary hemorrhagic telangiectasia (HHT), the second most common inherited bleeding disorder, is associated with the development of malformed blood vessels Abnormal blood vessels may be small and cutaneous or mucosal (telangiectasia), with frequent complications of bleeding, or large and visceral (arteriovenous malformations [AVMs]), with
- Hereditary haemorrhagic telangiectasia - DermNet
What causes hereditary haemorrhagic telangiectasia? The two major types of HHT are HHT1 and HHT2 They are caused by mutations in the endoglin (ENG) and activin receptor -like kinase type 1 (ACVLR1) genes found on chromosome 9 and 12 respectively
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