I. Guryanova, K. Skapavets, A. Liubushkin, E. Polyakova, I. Ausianik, S. Aleshkevich, A. Salivonchik, V. Vertelko, Y. Zharankova, M. Belevtsev
{"title":"Demographic characteristics of patients with genetically confirmed hereditary angioedema in the Republic of Belarus","authors":"I. Guryanova, K. Skapavets, A. Liubushkin, E. Polyakova, I. Ausianik, S. Aleshkevich, A. Salivonchik, V. Vertelko, Y. Zharankova, M. Belevtsev","doi":"10.14427/jipai.2022.2.12","DOIUrl":null,"url":null,"abstract":"Introduction. Hereditary angioedema (HAE) is a rare, difficult to diagnose, and life-threatening genetic disorder with an expected incidence of about 1:30 000. Purpose. To study the demographic characteristics in a cohort of patients with genetically confirmed hereditary angioedema in the Republic of Belarus. Materials and methods. The study included 92 Belarusian patients from 34 unrelated families with genetically confirmed HAE, the ratio of male and female patients was 1:1.3. Clinical and demographic data was taken from patient questionnaires and/or medical records. Results. The median age of tpatients was 32 years, and the median age at diagnosis was 28 years. The onset of the disease in 72% of patients occurred before the age of 18 years (median 13 years), the median delay from the onset of the first symptoms and the diagnosis of HAE was 12.5 years. Half of male patients develop first attacks before the age 9, and 90% by the age of 20. Of female patients, 50 and 90% have first attacks before the age of 15 and 23, respectively.","PeriodicalId":425120,"journal":{"name":"Immunopathology, Allergology, Infectology","volume":"30 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunopathology, Allergology, Infectology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14427/jipai.2022.2.12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction. Hereditary angioedema (HAE) is a rare, difficult to diagnose, and life-threatening genetic disorder with an expected incidence of about 1:30 000. Purpose. To study the demographic characteristics in a cohort of patients with genetically confirmed hereditary angioedema in the Republic of Belarus. Materials and methods. The study included 92 Belarusian patients from 34 unrelated families with genetically confirmed HAE, the ratio of male and female patients was 1:1.3. Clinical and demographic data was taken from patient questionnaires and/or medical records. Results. The median age of tpatients was 32 years, and the median age at diagnosis was 28 years. The onset of the disease in 72% of patients occurred before the age of 18 years (median 13 years), the median delay from the onset of the first symptoms and the diagnosis of HAE was 12.5 years. Half of male patients develop first attacks before the age 9, and 90% by the age of 20. Of female patients, 50 and 90% have first attacks before the age of 15 and 23, respectively.