Hereditary angioedema
Management of acute attacks of hereditary angioedema: role of ecallantide
... of angioedema are classified based on the mechanisms causing ...histaminergic angioedema and nonhistaminergic ...Histaminergic angioedema is typically associated with urticaria and histamine ...
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Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema
... Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is an autosomal dominant disorder; a form of bradykinin-mediated angioedema. It is charac- terized by recurrent, subcutaneous, and/or ...
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Management of Children With Hereditary Angioedema Due to C1 Inhibitor Deficiency
... Hereditary angioedema (HAE) is a potentially life-threatening inherited disease characterized by attacks of skin swelling, severe abdominal pain, and upper airway ...
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Hypersensitivity to Aspirin as a Factor for Poor Control in Hereditary Angioedema
... of angioedema of thebody and internal organs (tongue, larynx, bronchi, small intestine, large in- testine, ureter and in general any organ composed of smooth muscle), which may be manifested by isolated ...
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Diagnosis and screening of patients with hereditary angioedema in primary care
... Abstract: Hereditary angioedema (HAE) is a rare autosomal dominant disease that commonly manifests with episodes of cutaneous or submucosal angioedema and intense abdominal ...of angioedema ...
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New treatments addressing the pathophysiology of hereditary angioedema
... of angioedema in patients with C1-inhibitor ...of hereditary angioedema, and currently available agents used to treat hereditary angioedema prophylactically are ...of hereditary ...
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Socioeconomic burden of hereditary angioedema: results from the hereditary angioedema burden of illness study in Europe
... Background: Hereditary angioedema (HAE) due to C1 inhibitor deficiency is a rare but serious and potentially life-threatening disease marked by spontaneous, recurrent attacks of ...
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Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency
... Hereditary angioedema (HAE) is a rare and potentially life-threatening disease. It is characterized by non-pitting, non-pruritic swelling of subcutaneous or submucosal tis- sues of the skin, extremities, ...
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Food as a trigger for abdominal angioedema attacks in patients with hereditary angioedema
... Background: Hereditary angioedema with C1 inhibitor deficiency (C1-INH-HAE) is a rare inherited ...self-reported angioedema attacks associated with the ingestion of foodstuffs, administration of ...
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Hereditary angioedema: New therapeutic options for a potentially deadly disorder
... of hereditary angioedema (HAE) is fairly well understood today, the lag in diagnosis of a decade or more suggests that clinicians have low awareness of this ...
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Management of hereditary angioedema in pregnant women: a review
... of hereditary angioedema (HAE) have been described: two are due to C1 inhibitor (C1-INH) deficiency (C1-INH-HAE types I and II) and one is characterized by normal C1-INH ...of hereditary ...
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Successful use of daily intravenous infusion of C1 esterase inhibitor concentrate in the treatment of a hereditary angioedema patient with ascites, hypovolemic shock, sepsis, renal and respiratory failure
... Hereditary angioedema (HAE) is a rare autosomal dominant disease most commonly associated with defects in C1 esterase inhibitor (C1-INH). HAE manifests as recurrent episodes of edema in various body ...
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The establishment and utility of Sweha-Reg: a Swedish population-based registry to understand hereditary angioedema
... Methods: Sweha-Reg is a population-based registry of hereditary angioedema in Sweden with the objectives of providing epidemiological data, and so creates a framework for the study of this disease. The ...
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Management of upper airway edema caused by hereditary angioedema
... Hereditary angioedema (HAE) is a rare disorder of auto- somal dominant inheritance. Its genetic background involves mutation of the gene encoding the C1-inhibitor (C1-INH) or the factor XII protein (FXII) ...
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Self-administered C1 esterase inhibitor concentrates for the management of hereditary angioedema: usability and patient acceptance
... Abstract: Hereditary angioedema (HAE) is a rare genetic disease characterized by episodic subcutaneous or submucosal swelling. The primary cause for the most common form of HAE is a deficiency in functional ...
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Pediatric hereditary angioedema due to C1-inhibitor deficiency
... Hereditary angioedema (HAE) resulting from the deficiency of the C1 inhibitor (C1-INH) is a rare, life-threatening ...of angioedema involving the skin and/or the mucosa of the upper airways, as well ...
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The International/Canadian Hereditary Angioedema Guideline
... Canadian Hereditary Angioedema Guideline with an expanded scope to include the management of hereditary angioedema (HAE) patients ...Canadian Hereditary Angioedema ...registry. ...
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Canadian hereditary angioedema guideline
... with hereditary angioedema due to C1 inhibitor defi- ciency, the factors cited most often by both experts and patients as affecting their QoL included potentially life- threatening attacks; the adverse side ...
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Management of acute attacks of hereditary angioedema: potential role of icatibant
... acute hereditary angioedema. Hereditary angioedema, resulting from inherited partial C1 inhibitor deficiency, is a disabling condition characterized by intermittent episodes of ...
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Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
... Background: Hereditary angioedema caused by C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant ...18 angioedema patients and 13 healthy ...
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