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10 Possible Causes for Telangiectasia on Lips and Oral Mucosa, Von Willebrand Disease

  • Hereditary Hemorrhagic Telangiectasia

    Diagnosis HHT is a clinical diagnosis based on four features: Spontaneous, recurrent nosebleeds Telangiectasias of the lips, oral mucosa (inside the mouth), tongue, fingertips[texaschildrens.org] Von Willebrand's disease .[patient.info] Skin and mucosa Telangiectasias of the skin and mucosa are common among patients with hereditary hemorrhagic telangiectasia and usually affect the face, lips, tongue, oral[cmaj.ca]

  • Coagulation Abnormalities

    People with this disorder have small red-to-violet telangiectatic lesions on the face, lips, oral and nasal mucosa, and tips of the fingers and toes.[msdmanuals.com] Here you will find information on inherited bleeding disorders, such as hemophilia, von Willebrand disease and rare factor deficiencies.[hemophilia.org] […] factor deficiency - Factor XIII afibrinogenaemia Links: haemophilia A von Willebrand's disease (congenital deficiency of von Willebrand's factor ) haemophilia B factor XI[gpnotebook.co.uk]

  • Hereditary Coagulopathy

    People with this disorder have small red-to-violet telangiectatic lesions on the face, lips, oral and nasal mucosa, and tips of the fingers and toes.[msdmanuals.com] KeyWords: von Willebrand disease, von Willebrand factor, hemostasis RESUMO A doença de von Willebrand (DvW) é uma coagulopatia hereditária. Não há predileção por sexo.[scielo.br] Please be sure to visit your local CSLBehring.com site for further information. von Willebrand Disease Von Willebrand Disease (VWD) is a bleeding disorder caused by a deficiency[allaboutbleeding.com]

  • Iron Deficiency

    Pigmentation of the lips and oral mucosa, which may suggest Peutz-Jeghers syndrome.[patient.info] Willebrand disease End-stage renal failure – combination of blood loss from dialysis and low erythropoietin levels (hormone that stimulates red blood cell production) Congestive[dermnetnz.org] Family history and genetics - Iron-Deficiency Anemia Von Willebrand disease is an inherited bleeding disorder that affects the blood’s ability to clot.[nhlbi.nih.gov]

  • Hemoptysis

    Telangiectasia, especially on the lips or buccal mucosa, may raise the diagnosis of hereditary hemorrhagic telangiectasia.[antimicrobe.org] Willebrand’s Disease, thrombocytopenia, anticoagulants) Immune/Vasculitis (Henoch-Shonlein Purpura, Wegener’s, Goodpasture’s, SLE) Pulmonary Vasculature Disorder (PE, AVM[pedclerk.bsd.uchicago.edu] Willebrand disease Haemophilia Anticoagulant therapy Thrombocytopenia Platelet dysfunction Disseminated intravascular coagulation Vasculitis Behcet’s disease Granulomatosis[lifeinthefastlane.com]

  • Microcytic Anemia

    Pigmentation of the lips and oral mucosa, which may suggest Peutz-Jeghers syndrome.[patient.info] ., von Willebrand disease).[aafp.org] Multiple telangiectasias, which may be a feature of hereditary haemorrhagic telangiectasia, also known as Osler-Weber-Rendu syndrome.[patient.info]

  • X-Linked Mandibulofacial Dysostosis

    Mucosa Isolated cleft palate and cleft lip with or without cleft palate, Hereditary hemorrhagic telangiectasia, Multiple mucosal neuroma syndrome, Neurofibromatosis of von[quizlet.com] Willebrand disease VWF, GP1BA Mild mucocutaneous bleeding, bruising without recognized trauma, menorrhagia 0.1% to 1% of the population Early onset, rare late onset[centogene.com] An autosomal dominant inheritance pattern, Occur on the buccal aspect of the maxilla, May be single, multiple, unilateral, or bilateral Inherited Disorders Affecting the Oral[quizlet.com]

  • Acquired Disorder

    People with this disorder have small red-to-violet telangiectatic lesions on the face, lips, oral and nasal mucosa, and tips of the fingers and toes.[merckmanuals.com] Willebrand disease autoimmune responses thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS) liver failure kidney failure paraproteinemia disseminated[healthline.com] Please be sure to visit your local CSLBehring.com site for further information. von Willebrand Disease Von Willebrand Disease (VWD) is a bleeding disorder caused by a deficiency[allaboutbleeding.com]

  • Hereditary Hemorrhagic Telangiectasia Type 2

    Small red-to-violet lesions are found on the lips, oral and nasal mucosa, tongue, and tips of fingers and toes.[medical-dictionary.thefreedictionary.com] What is Von Willebrand Disease? National Heart, Lung and Blood Institute.Available online at May 2017. (2012 March 14). What is Immune Thrombocytopenic Purpura?[labtestsonline.it] Von Willebrand's disease.[patient.info]

  • Glomerulonephritis - Sparse Hair - Telangiectasis Syndrome

    (pulmonary disease in type I type II) Cutaneous findings • Multiple macular/ “mat-like” telangiectasias most commonly on lips, oral mucosa , and extremities ( Fig. 10-2 )[plasticsurgerykey.com] Hippel-Lindau syndrome Von Willebrand Disease, Type I Von Willebrand Disease, Type IIB Von Willebrand Disease, Type IIM Von Willebrand Disease, Type III Waardenburg Syndrome[sequencing.com] Figure 10-2 Patient with HHT and multiple telangiectasias on tongue and lip.[plasticsurgerykey.com]

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