Hereditary Angioedema: A Case Report
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Case Report
P: 29-31
December 2004

Hereditary Angioedema: A Case Report

İstanbul Med J 2004;5(4):29-31
1. İstanbul Eğitim ve Araştırma Hastanesi, 2. İç Hastalıkları Kliniği, Asistanı
2. SSK İstanbul Eğitim Hastanesi İç Hastalıkları Uzmanı
3. SSK İstanbul Hastanesi 4. Dahiliye Kliniği
4. SSK İstanbul Eğitim Hastanesi, İç Hastalıkları Uzmanı
5. SSK İstanbul Hastanesi İç Hastalıkları Kliniği, Şefi
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ABSTRACT

Hereditary angioedema is an rare autosomal dominant disease which affects respiratory, gastrointestinal and subcutaneus tissues. This condition is due to an inherited deficiency of C1 esterase inhibitor. Hereditary angioedema can be associated with autoimmun disease such as, systemic lupus erythematosus, rheumatoid artritis, autoimmun thyroiditis and glomerulonephritis. It may also occur with infections, travma, stress and the changes of the temperature. Our case seems to be interesting because the disease is rare and had been diagnosed in a late age.

Keywords: Hereditary angioedema, C1 esterase inhibitor

References

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