ArticleAllergy, asthma & immunology research2013
A case of hereditary angioedema in a 7-year-old korean girl.
Article in Allergy, asthma & immunology research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 8 citations in OpenAlex.
- Angioedema in a 9-year-old Child after Dental Treatment: A Rare Complication Explored through a Case Report.International journal of clinical pediatric dentistry · 2024Article
- Complement 4 levels of a 4-year-old girl with angioedema.Clinical and experimental pediatrics · 2020Article
- A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation.Allergy, asthma & immunology research · 2017Article
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Authors and funding
2 authors at 2 institutions in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
Hereditary angioedema (HAE) is a rare autosomal dominant disease that usually occurs in adolescence and early adulthood. It is characterized by recurrent non-pitting edema involving the skin and intestinal tract, especially the extremities and face. It is not associated with urticaria and pruritus. The cause is known to be the deficiency of C1 inhibitor. We herein report a 7-year-old girl with HAE who had recurrent episodes of swelling of the extremities and face without urticaria and pruritus. Her great grandmother had suffered from the same symptoms. The level of serum C4 was 8.01 mg/dL (normal: 10-40 mg/dL). The level of C1 inhibitor was 5.0 mg/dL (normal: 18-40 mg/dL). To our knowledge, this is the first pediatric case with typical clinical symptoms of HAE and C1 esterase inhibitor deficiency in Korea.
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