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107 Possible Causes for Hereditary Hemorrhagic Telangiectasia, Telangiectasis

  • Hereditary Hemorrhagic Telangiectasia

    Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family history, recurrent nosebleeds, mucocutaneous telangiectasis, and arteriovenous[] Symptomatic Children with Hereditary Hemorrhagic Telangiectasia.[] These abnormal blood vessels are called telangiectasis if they involve small blood vessels (nose, stomach and small bowel) and arterioveneous malformations (AVM) if it involves[]

  • Pulmonary Arteriovenous Fistula

    In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis[] He had diffuse telangiectasia of the tongue, and hereditary hemorrhagic telangiectasia was diagnosed.[] […] arteriovenous fistulae. 44 The association of hemorrhagic telangiectasias with pulmonary arteriovenous fistulae has been amply confirmed. 4, 5, 18, 19 Hereditary hemorrhagic telangiectasis[]

  • Generalized Essential Telangiectasia

    A syndrome characterised by choreoathetosis beginning in childhood, progressive cerebellar ataxia, telangiectasis of conjunctiva and skin, slowly progressive mental deterioration[] Recurrent hemorrhage in the setting of telangiectases, including GI bleeding, is more typically associated with hereditary hemorrhagic telangiectasia.[] Other primary telangiectases include angioma serpiginosum , ataxia- telangiectasia and spider telangiectasis .[]

  • Cerebral Arteriovenous Malformation

    Benign proliferating vascular anomalies Haemangioma Non-proliferating vascular anomalies Capillary malformation (telangiectasis) Venous malformation (developmental venous[] Cerebral arteriovenous malformations (AVMs) are associated with hereditary hemorrhagic telangiectasia (HHT).[] Patients with hereditary hemorrhagic telangiectasia (HHT) are at risk for the development of cerebral arteriovenous malformations (AVMs).[]

  • Colonic Angiodysplasia

    GI angiodysplasia has been reported to be associated with other systemic diseases, such as aortic valvular diseases, systemic sclerosis, hereditary hemorrhagic telangiectasis[] hemorrhagic telangiectasia) 10 Asymptomatic Presentation GIB (1) Major bleed (2) Recurrent minor bleed (3) Positive FOB 11 Introduction Diagnosis Management Controversial[] Hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) is an autosomal dominant disorder that causes multiple vascular lesions in various parts of the body, including[]

  • Rosacea

    In a fair, delicate skin predisposed to rosacea, anything that makes one flush will promote rosacea and telangiectasis.[] These include Rothmund-Thomson syndrome, Bloom syndrome, Cockayne syndrome, ataxia-telangiectasia and hereditary hemorrhagic telangiectasia [ 79 – 85 ].[] Symptoms of rosacea The symptoms of rosacea include: enlarged capillaries (telangiectasis) a permanent flush across the nose and cheeks yellow-headed pimples on the forehead[]

  • Pulmonary Arteriovenous Malformation

    Following magnetic resonance angiogram and chest CT as well as noting multiple telangiectasis on her skin and considering a strong family history, Osler-Weber-Rendu syndrome[] hemorrhagic telangiectasia syndrome (HHT).[] The diagnosis of PAVM should be suspected in individuals presenting with telangiectasis on mucous membranes or skin and unexplained clinical manifestations such as hypoxia[]

  • Limited Cutaneous Systemic Sclerosis

    Sixteen cases of SS or CREST treated with PDL between 1997 and 2007 were evaluated and response to treatment was compared with 20 patients with sporadic telangiectasis.[] Abstract A 64-year-old woman with CREST syndrome developed prominent telangiectases mimicking hereditary hemorrhagic telangiectasia (HHT) of Osler-Rendu-Weber.[] He presented with erythema, tight skin over his face and digits, subcutaneous calcification, telangiectasis, as well as Raynaud's phenomenon.[]

  • Liver Disease

    A Sri Lankan girl with hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) is described.[] We report a case of a 62-year-old woman who received a liver transplant 19 years previously for end-stage liver disease due to hereditary hemorrhagic telangiectasia and fibropolycystic[] A diagnosis of Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) was made based on the presence of three Curacao criteria (out of four).[]

  • Hemangioma

    McAllister KAGrogg KMJohnson DW Endoglin, a TGF-β binding protein for endothelial cells, is the gene for hereditary hemorrhagic telangiectasia.[] Associations extrahepatic hemangiomata hereditary hemorrhagic telangiectasia ( Osler-Weber-Rendu disease ) Kasabach-Merritt syndrome : with giant hemangiomas hepatic arterioportal[] These include Rothmund-Thomson syndrome, Bloom syndrome, Cockayne syndrome, ataxia-telangiectasia and hereditary hemorrhagic telangiectasia [ 79 – 85 ].[]

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