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1,928 Possible Causes for Angioedema

  • Angioedema

    Drug-induced angioedema is more common in African-American. Annually 80000 to 112000 patients suffering from angioedema visit emergency department.[] Drug-induced angioedema Gleich's syndrome (unexplained angioedema with high eosinophil counts) Ruconest (C1-inhibitor) Angioedema at Curlie[] A number of foods and drugs can precipitate allergic angioedema.[]

  • Laryngeal Edema

    Laryngeal edema in hereditary angioedema may be fatal.[] Recurrent angioedema is the hallmark of various inherited or acquired angioedema diseases.[] BACKGROUND: Hereditary angioedema (HAE) is an autosomal dominant disease (Mendelian Inheritance in Man 106100) caused by an inherited deficiency of C1 inhibitor (C1-INH) function[]

  • Anaphylaxis

    Hives and angioedema (hives on the lips, eyelids, throat, and/or tongue) often occur, and angioedema may be severe enough to cause obstruction of the airway.[] Here, we present a 48-year-old woman without significant medical and family history with recurrent angioedema in the setting of catamenial anaphylaxis or cyclical anaphylaxis[] Site involvement as a predictor of airway intervention in angioedema. Laryngoscope. 2011;121:262–266. PMID 21271571 Pumphrey RS.[]

  • Urticaria

    A family history of hives or angioedema Autoimmune disease such as lupus or Hashimoto's thyroiditis , for which angioedema is a possible symptom If you or a loved one have[] Rarer causes are hereditary angioedema (HAE) or acquired angioedema (AAE).[] With non-immunologic angioedema, the immune system has nothing to do with the release.[]

  • Acquired Angioedema

    This represents a rare case of a patient with hereditary angioedema who developed acquired angioedema due to a lymphoma that was associated with a reduction in the levels[] […] shown to be effective in hereditary angioedema, was undertaken.[] Abstract Acquired angioedema (AAE) is a rare disorder that has been categorized into two forms, AAE-I and AAE-II.[]

  • Nonallergic Urticaria

    Figure 2 Angioedema of the lips (5) Figure 3 Angioedema of the hand (6) Symptoms can occur singly or in combination; acute urticaria presents with angioedema in about 50%[] What else can cause angioedema?[] Sometimes, hives will occur along with significant swelling, called angioedema, although angioedema can also occur by itself.[]

  • Hereditary Angioedema

    Hereditary angioedema is a disorder characterized by recurrent episodes of severe swelling (angioedema).[] Hereditary angioedema (HAE) is an autosomal dominant disorder that involves a defect in the C1-INH protein. A detailed history concerning angioedema should be done.[] Abdelmalek MFDouglas DD Lisinopril-induced isolated visceral angioedema: review of ACE-inhibitor–induced small bowel angioedema.[]

  • Hereditary Angioedema Type 1

    Hereditary angioedema (HAE) is a rare genetic disease that affects approximately 1 in 50,000 individuals and is classified into three types.[] Idiopathic angioedema Description of Idiopathic angioedema Idiopathic angioedema is the most common type of angioedema and can occur in anyone at any age.[] "Hereditary Angioedema." Medscape. Updated: Feb 25, 2015. 2. US Hereditary Angioedema Association. "About Hereditary Angioedema."[]

  • Hypereosinophilic Syndrome

    Clinical description Target-organ damage mediated by eosinophils is highly variable among patients, and consists of dermatological involvement (urticaria, eczema, angioedema[] Other hypereosinophilic syndrome variants include chronic eosinophilic leukemia, Gleich syndrome (cyclical eosinophilia and angioedema), familial hypereosinophilic syndrome[] These manifestations include:Skin rashes, for example, urticaria or angioedema, Dizziness, Memory misfortune or disarray, Cough, Shortness of inhale, Fatigue, Fever, Mouth[]

  • Hypocomplementemic Vasculitis

    Cyclic citrullinated peptide antibody, U C3 complement, mg/dL 50 90-180 C4 complement, mg/dL 3 16-47 CH50, U/mL 31-66 Antineutrophil cytoplasmic antibody Negative Negative Angioedema[] We report a patient who developed recurrent urticaria and angioedema at age 2 years, severe hypocomplementemic glomerulonephritis at 11 years, and end-stage renal disease[] Breathing difficulty * Chronic urticarial vasculitis * Chronic hypocomplementemia * Joint pain Causes - Hypocomplementemic urticarial vasculitis * Idiopathic urticaria without angioedema[]

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