Literature DB >> 11855162

A case of hereditary angioedema associated with idiopathic hypoparathyroidism.

S H Kim1, B J Lee, Y S Chang, Y K Kim, S H Cho, K U Min, Y Y Kim.   

Abstract

Hereditary angioedema is a rare autosomal dominant disease characterized by the edema of subcutaneous tissues, respiratory tract and bowel. It is caused by the deficiency of C1 esterase inhibitor. Hereditary angioedema may be associated with autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, autoimmune thyroiditis and glomerulonephritis. We report a 34-year-old male patient with hereditary angioedema who developed idiopathic hypoparathyroidism. Autoimmunity seems to be an important basis of this association and it might be caused by the immune dysfunction due to decreased level of complements; nevertheless, a casual association could not be excluded. To our knowledge, this is the first report of hereditary angioedema in association with idiopathic hypoparathyroidism in the medical literature.

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Year:  2001        PMID: 11855162      PMCID: PMC4578060          DOI: 10.3904/kjim.2001.16.4.281

Source DB:  PubMed          Journal:  Korean J Intern Med        ISSN: 1226-3303            Impact factor:   2.884


  11 in total

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  2 in total

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Authors:  Meeyong Shin; Kangmo Ahn
Journal:  Allergy Asthma Immunol Res       Date:  2012-08-23       Impact factor: 5.764

2.  A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation.

Authors:  Da Woon Sim; Kyung Hee Park; Jae Hyun Lee; Jung Won Park
Journal:  Allergy Asthma Immunol Res       Date:  2017-01       Impact factor: 5.764

  2 in total

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