Hht.org is a foundation for Hereditary Hemorrhagic Telangiectasia
Title
HHT.org: Hereditary Hemorrhagic Telangiectasia | Osler-Weber-Rendu Syndrome
Description
The HHT Foundation was formed in 1990 to aid and support persons with Hereditary Hemorrhagic Telangiectasia (HHT) also known as Osler-Weber-Rendu Syndrome; to provide patients, families and doctors with educational information; to foster an exchange of information about the diagnosis and treatment of HHT between patients, physicians, researchers, genetic counselors, charitable organizations, government agencies, industry, academic institutions and the general public; to raise funds for genetic and clinical research and for sponsoring special scholarships for studies pertaining to HHT.
Contact
- Reflect Web Design Services
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- N/A N/A
- United States N/A
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- +1.8004486389
