{"title":"无声的咬伤:遭遇毒蛇后揭开因子 XII 缺陷的面纱","authors":"Srutdi Kamalam Natarajan, Sairaksha Sudhakar, Devasena Srinivasan","doi":"10.36106/ijar/9704330","DOIUrl":null,"url":null,"abstract":"Factor 12 or the Hageman factor plays an essential role in the initiation of the intrinsic or the contact pathway of\ncoagulation. The activation of the pathway occurs either due to direct contact with a negatively charged surface like glass\nor kaolin or proteolytic activation through prekallikrein and kallikrein system. Activated partial thromboplastin time or aPTT clotting assay is the\ntest which is used to evaluate the status of the intrinsic pathway. Factor 12 deciency is a rare genetic disorder which usually follows an autosomal\nrecessive pattern of inheritance however an autosomal dominant inheritance has also been reported. There is no established data regarding the\nprevalence of Factor 12 deciency in the normal population. Based on a study conducted on 300 healthy blood donors, an estimated prevalence of\n2.3% has been reported according to Halbmayer WM, et al. The incidence of the condition is about 1 in 1,000,000 individuals. In patients with a\ndeciency of Factor 12, the aPTT is typically prolonged and there are no associated bleeding tendencies. More often there is an increased risk of\narterial or venous thromboembolic events and the patient is usually asymptomatic according to Chaudhry LA, et al.","PeriodicalId":13502,"journal":{"name":"Indian journal of applied research","volume":"199 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A SILENT BITE : FACTOR XII DEFICIENCY UNMASKED IN THE WAKE OF A SNAKE ENCOUNTER\",\"authors\":\"Srutdi Kamalam Natarajan, Sairaksha Sudhakar, Devasena Srinivasan\",\"doi\":\"10.36106/ijar/9704330\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Factor 12 or the Hageman factor plays an essential role in the initiation of the intrinsic or the contact pathway of\\ncoagulation. The activation of the pathway occurs either due to direct contact with a negatively charged surface like glass\\nor kaolin or proteolytic activation through prekallikrein and kallikrein system. Activated partial thromboplastin time or aPTT clotting assay is the\\ntest which is used to evaluate the status of the intrinsic pathway. Factor 12 deciency is a rare genetic disorder which usually follows an autosomal\\nrecessive pattern of inheritance however an autosomal dominant inheritance has also been reported. There is no established data regarding the\\nprevalence of Factor 12 deciency in the normal population. Based on a study conducted on 300 healthy blood donors, an estimated prevalence of\\n2.3% has been reported according to Halbmayer WM, et al. The incidence of the condition is about 1 in 1,000,000 individuals. In patients with a\\ndeciency of Factor 12, the aPTT is typically prolonged and there are no associated bleeding tendencies. More often there is an increased risk of\\narterial or venous thromboembolic events and the patient is usually asymptomatic according to Chaudhry LA, et al.\",\"PeriodicalId\":13502,\"journal\":{\"name\":\"Indian journal of applied research\",\"volume\":\"199 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian journal of applied research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36106/ijar/9704330\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian journal of applied research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36106/ijar/9704330","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A SILENT BITE : FACTOR XII DEFICIENCY UNMASKED IN THE WAKE OF A SNAKE ENCOUNTER
Factor 12 or the Hageman factor plays an essential role in the initiation of the intrinsic or the contact pathway of
coagulation. The activation of the pathway occurs either due to direct contact with a negatively charged surface like glass
or kaolin or proteolytic activation through prekallikrein and kallikrein system. Activated partial thromboplastin time or aPTT clotting assay is the
test which is used to evaluate the status of the intrinsic pathway. Factor 12 deciency is a rare genetic disorder which usually follows an autosomal
recessive pattern of inheritance however an autosomal dominant inheritance has also been reported. There is no established data regarding the
prevalence of Factor 12 deciency in the normal population. Based on a study conducted on 300 healthy blood donors, an estimated prevalence of
2.3% has been reported according to Halbmayer WM, et al. The incidence of the condition is about 1 in 1,000,000 individuals. In patients with a
deciency of Factor 12, the aPTT is typically prolonged and there are no associated bleeding tendencies. More often there is an increased risk of
arterial or venous thromboembolic events and the patient is usually asymptomatic according to Chaudhry LA, et al.