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  2. Acquired C1 esterase inhibitor deficiency - Wikipedia

    en.wikipedia.org/wiki/Acquired_C1_esterase...

    However, it is thought that this disease prevalence could be higher due to diagnostic oversight and the shared symptoms of acquired angioedema with similar diseases. [5] This disease tends to affect males and females equally. [4] Additionally, individuals with acquired angioedema usually develop symptoms in their fourth decade of life or older. [4]

  3. Hereditary angioedema - Wikipedia

    en.wikipedia.org/wiki/Hereditary_angioedema

    Normal C1 inhibitor level hereditary angioedema is thought to involve various mutations that increased bradykinin activity and cause a decreased threshold for activation of the plasma contact system thus leading to the symptoms of angioedema. [7] Hereditary angioedema with normal C1-inhibitor is a genetically heterogeneous disorder.

  4. Angioedema - Wikipedia

    en.wikipedia.org/wiki/Angioedema

    Angioedema can be due to antibody formation against C1INH; this is an autoimmune disorder. This acquired angioedema is associated with the development of lymphoma. Consumption of foods that are themselves vasodilators, such as alcoholic beverages or cinnamon, can increase the probability of an angioedema episode in susceptible patients. If the ...

  5. Classical complement pathway - Wikipedia

    en.wikipedia.org/wiki/Classical_complement_pathway

    Lack of regulation of the classical complement pathway through the deficiency in C1-inhibitor results in episodic angioedema. [1] C1-inhibitor defiency can be hereditary or acquired, resulting in hereditary or acquired angioedema. [12] C1-inhibitor plays the role of inactivating C1r and C1s to prevent further downstream classical complement ...

  6. Complement deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_deficiency

    Disorders of the proteins that act to inhibit the complement system (such as C1-inhibitor) can lead to an overactive response, causing conditions such as hereditary angioedema. [8] Disorders of the proteins that act to activate the complement system (such as C3) can lead to an underactive response, causing greater susceptibility to infections. [9]

  7. Chronic spontaneous urticaria - Wikipedia

    en.wikipedia.org/wiki/Chronic_spontaneous_urticaria

    Angioedema, excruciatingly itchy recurrent wheals, or both can be signs of chronic spontaneous urticaria. [5] Between 40 and 50 percent of CSU patients experience angioedema. [6] However, angioedema is the main symptom reported by about 10% of patients. [7] Usually, urticarial lesions or hives are elevated, erythematous plaques with a defined ...

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