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  2. 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.

  3. Angioedema - Wikipedia

    en.wikipedia.org/wiki/Angioedema

    The hereditary form (HAE) often goes undetected for a long time, as its symptoms resemble those of more common disorders, such as allergy or intestinal colic. An important clue is the failure of hereditary angioedema to respond to antihistamines or steroids, a characteristic that distinguishes it from allergic reactions. It is particularly ...

  4. Acquired C1 esterase inhibitor deficiency - Wikipedia

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

    Typically, acquired angioedema presents later in adulthood, in contrast to hereditary angioedema which usually presents from early childhood and with similar symptoms. [2] Acquired angioedema is usually found after recurrent episodes of swelling and can in some cases take several months to diagnose.

  5. 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]

  6. Remitting seronegative symmetrical synovitis with pitting edema

    en.wikipedia.org/wiki/Remitting_seronegative...

    Remitting seronegative symmetrical synovitis with pitting edema (or sometimes RS 3 PE) is a rare syndrome identified by symmetric polyarthritis, synovitis, acute pitting edema (swelling) of the back of the hands and/or feet, and a negative serum rheumatoid factor. [2]

  7. Primary immunodeficiency - Wikipedia

    en.wikipedia.org/wiki/Primary_immunodeficiency

    The precise symptoms of a primary immunodeficiency depend on the type of defect. Generally, the symptoms and signs that lead to the diagnosis of an immunodeficiency include recurrent or persistent infections or developmental delay as a result of infection. Particular organ problems (e.g. diseases involving the skin, heart, facial development ...

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