2020
DOI: 10.1016/j.oooo.2020.08.038
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Hereditary angioedema: Report of the dental treatment of 12 Brazilian patients

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“…It has a chronic and disabling course and is difficult to diagnose without specialized evaluation. Diagnosis can be delayed up to 15 years after symptom onset ( 1 ). HAE is inherited as an autosomal dominant trait caused by a mutation in the C1-inhibitor gene on chromosome 11.…”
Section: Introductionmentioning
confidence: 99%
“…It has a chronic and disabling course and is difficult to diagnose without specialized evaluation. Diagnosis can be delayed up to 15 years after symptom onset ( 1 ). HAE is inherited as an autosomal dominant trait caused by a mutation in the C1-inhibitor gene on chromosome 11.…”
Section: Introductionmentioning
confidence: 99%