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Lesions lips, patient with hemorrhagic hereditary telangiectasia. 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 (Osler–Weber–Rendu syndrome) Ataxia–telangiectasia Sturge–Weber syndrome , a nevus formation in the skin supplied by the trigeminal nerve and associated with facial port-wine stains, glaucoma , meningeal angiomas and intellectual disabilities
Hereditary hemorrhagic telangiectasia; Hereditary nonpolyposis colorectal cancer; Heyde's syndrome; I. Irritable bowel syndrome; J. Johanson–Blizzard syndrome;
Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Hereditary hemorrhagic telangiectasia. PubMed provides review articles from the past five years (limit to free review articles)
Hereditary hemorrhagic telangiectasia is a condition where there is direct connection between arterioles and venules without intervening capillary beds, at the mucocutaneous region and internal bodily organs. Those who are affected by this conditions usually do not experience any symptoms.
Hereditary hemorrhagic telangiectasia, or Rendu-Osler-Weber disease; Hilbert–Huang transform; Hiphop Tamizha, an Indian musical duo; Historic House Trust of New York City; Historic Houses Trust, New South Wales; Omega-hydroxypalmitate O-feruloyl transferase, an enzyme; Howard Thompson (film critic), who wrote under the pen name HHT
In contrast, loss-of-function (LOF) mutations in SMAD4 predispose individuals to gastrointestinal polyps, a higher risk of colorectal cancer, and a risk of forming arteriovenous malformations (AVM) a hallmark manifestation of hereditary hemorrhagic telangiectasia (HHT). [8] Patients also have external phenotypes similar to Marfan syndrome. [9]
Telangiectasia ataxia variant V1; Telangiectasia, hereditary hemorrhagic; Telangiectasia; Telecanthus hypertelorism pes cavus; Telecanthus with associated abnormalities; Telencephalic leukoencephalopathy; Telfer–Sugar–Jaeger syndrome; Temporal epilepsy, familial; Temporomandibular ankylosis; Temporomandibular joint dysfunction (TMJ) Temtamy ...