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  2. Hereditary angioedema - Wikipedia

    en.wikipedia.org/wiki/Hereditary_angioedema

    Hereditary angioedema (HAE) is a disorder that results in recurrent attacks of severe swelling. [3] The swelling most commonly affects the arms, legs, face, intestinal tract, and airway. [3]

  3. List of autoimmune diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_autoimmune_diseases

    This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the body. Each disorder is listed with the primary organ or body part that it affects and the associated autoantibodies that are typically found in people diagnosed ...

  4. Microscopic polyangiitis - Wikipedia

    en.wikipedia.org/wiki/Microscopic_polyangiitis

    Clinical features may include constitutional symptoms like fever, arthralgia, myalgia, loss of appetite, weight loss and fatigue.A variety of organs can be affected, which causes a wide range of symptoms such as cough, shortness of breath, hemoptysis (coughing up of blood), symptoms of kidney failure, skin manifestations (palpable purpura and livedo racemosa [1]), seizures or peripheral ...

  5. Angioedema - Wikipedia

    en.wikipedia.org/wiki/Angioedema

    Angioedema is an area of swelling of the lower layer of skin and tissue just under the skin or mucous membranes. [1] [3] The swelling may occur in the face, tongue, larynx, abdomen, or arms and legs. [1] Often it is associated with hives, which are swelling within the upper skin. [1] [3] Onset is typically over minutes to hours. [1]

  6. 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]

  7. Autoimmune disease - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_disease

    The exact causes of autoimmune diseases remain unclear and are likely multifactorial, involving both genetic and environmental influences. [7] While some diseases like lupus exhibit familial aggregation, suggesting a genetic predisposition , other cases have been associated with infectious triggers or exposure to environmental factors, implying ...

  8. Chronic spontaneous urticaria - Wikipedia

    en.wikipedia.org/wiki/Chronic_spontaneous_urticaria

    Chronic spontaneous urticaria, despite its cause being unknown, is linked to a higher prevalence of autoimmune diseases, and is often worsened by triggers like stress, infections, certain foods, or nonsteroidal anti-inflammatory drugs. The hives and angioedema seen in CSU is thought to be linked to the degranulation of skin mast cells.

  9. Remitting seronegative symmetrical synovitis with pitting edema

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

    Other rheumatological disorders that can cause the features typical for RS3PE include late onset (seronegative) rheumatoid arthritis, acute sarcoidosis, ankylosing spondylitis and other spondyloarthropathies such as psoriatic arthropathy, mixed connective tissue disease, chondrocalcinosis and arthropathy due to amyloidosis. [6] [9]