ArticleThe Korean journal of internal medicine2001
A case of hereditary angioedema associated with idiopathic hypoparathyroidism.
Article in The Korean journal of internal medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed, 7 citations in OpenAlex.
- A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation.Allergy, asthma & immunology research · 2017Article
- A case of hereditary angioedema in a 7-year-old korean girl.Allergy, asthma & immunology research · 2013Article
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Authors and funding
7 authors at 3 institutions in 2 countries.
Funding
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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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