Abstract
This current clinical case report highlights three cases of Hereditary angioedema (HAE) patients who are all members of the same family (father and his two daughters). The father has C1âINH deficiency, while his daughters have low C1âINH levels: the first possesses only 10% function and the second has low C1âINH level with 0% function. Of note, the second daughter was discovered to have HAE at the age of 2, thus making her the youngest known HAE case report in the English literature.
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