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Mashup Score: 1Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variation - 2 year(s) ago
Key Points. We tested 75 HHT-independent genes by whole genome sequencing, integrating clinical severity classifications and population variant burdens.We show
Source: American Society of HematologyCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 4UF Health named HHT Center of Excellence - CureHHT - 2 year(s) ago
Cure HHT is excited to announce that UF Health has been named the first HHT Center of Excellence in Florida and the 31st CoE in North America.Cure HHT recognizes hospitals equipped with the personnel, expertise, commitment and resources to provide comprehensive evaluation, treatment and education to individuals with HHT and their families. Recognition as an HHT CoE follows 18 months of training,…
Source: CureHHTCategories: Latest Headlines, Rare DiseaseTweet
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Mashup Score: 0Public Health Webinar Series | Blood Disorders | NCBDDD | CDC - 2 year(s) ago
CDC’s Division of Blood Disorders (DBD) is proud to offer its Public Health Webinar Series on Blood Disorders. Learn more.
Categories: Latest Headlines, PediatricsTweet
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Mashup Score: 0Facts About Hereditary Hemorrhagic Telangiectasia (HHT) - 2 year(s) ago
A person with HHT may form blood vessels without the capillaries that are usually present between arteries and veins.
Categories: Latest Headlines, PediatricsTweet-
#DYK 90% of people living with HHT are undiagnosed? #HHT is a genetic disorder that causes abnormally-formed blood vessels. Signs can include: -Nosebleeds -Red/Purplish spots on the skin -Stomach or intestinal bleeding Learn more for #HHTAwarenessMonth: https://t.co/7VEe6AIwvP https://t.co/U3JNtlN52w
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Mashup Score: 0Facts About Hereditary Hemorrhagic Telangiectasia (HHT) - 2 year(s) ago
A person with HHT may form blood vessels without the capillaries that are usually present between arteries and veins.
Categories: Latest Headlines, PediatricsTweet-
#DYK 90% of people living with HHT are undiagnosed? #HHT is a genetic disorder that causes abnormally-formed blood vessels. Signs can include: -Nosebleeds -Red/Purplish spots on the skin -Stomach or intestinal bleeding Learn more for #HHTAwarenessMonth: https://t.co/7VEe6AIwvP https://t.co/q6OTjF0dto
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Mashup Score: 0Federal Funding Secured for U.S. Centers of Excellence - CureHHT - 2 year(s) ago
A message from Cure HHT Executive Director, Marianne Clancy It is with tearful joyfulness that I share this truly momentous news with you: Our HHT Center of Excellence (CoE) funding request made it into the final spending bill, and that bill was signed into law by President Biden just a few weeks ago. At long…
Source: CureHHTCategories: Latest Headlines, Rare DiseaseTweet
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Mashup Score: 3Federal Funding Secured for U.S. Centers of Excellence - CureHHT - 2 year(s) ago
A message from Cure HHT Executive Director, Marianne Clancy It is with tearful joyfulness that I share this truly momentous news with you: Our HHT Center of Excellence (CoE) funding request made it into the final spending bill, and that bill was signed into law by President Biden just a few weeks ago. At long…
Source: CureHHTCategories: Latest Headlines, Rare DiseaseTweet
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Mashup Score: 2
Hanny Al-Samkari, M.D. Massachusetts General Hospital Boston, Massachusetts, U.S. On Tuesday, July 20, 2021, Hanny Al-Samkari, M.D., of Massachusetts General Hospital in Boston presented results on oral pazopanib for severe hereditary hemorrhagic telangiectasia (HHT)-associated bleeding. HHT, also known as Osler‐Weber‐Rendu syndrome, is a relatively common (1 in 5,000 persons), under‐recognized…
Source: ISTH Congress Daily 2021Categories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 1Treatment of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia - a Case Series and Systematic Review - PubMed - 3 year(s) ago
Twenty-one articles were selected. Studies were before-and-after observational studies, case reports, and case series. Among all subjects with HHT-PAH, both mPAP (65±19 pre-treatment vs 51±16 mmHg post-treatment p=0.04) and PVR (12±6 pre-treatment vs 8±4 WU post-treatment p=0.01) improved with treat …
Source: PubMedCategories: Latest Headlines, PulmonologyTweet
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Mashup Score: 0
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease, affecting approximately 1 in 8000 and complicated by vascular malformations (VMs).1,2 Patients are at risk of life-threatening complications from VMs in the lungs and brain, which can be treated preventatively.3 We report here the current routine screening practice for lung and brain VMs across North American HHT…
Source: SAGE JournalsCategories: Cardiology News and Journals, Latest HeadlinesTweet
Complex paper published in @BloodAdvances shows that patients with Hereditary Hemorrhagic Telangiectasia (#HHT) are more likely to bleed if they have abnormalities in other coagulation/platelet genes. I bet it will be the same in type 1 VWD. https://t.co/bN71PxOsQ8 https://t.co/3HVNyc1AWg