{"title":"571年诊断为希佩尔-林道病的年轻病人一例C >g突变(克罗埃西亚型)和多发性副神经节瘤","authors":"K. Blažina","doi":"10.15406/MOJCR.2021.11.00373","DOIUrl":null,"url":null,"abstract":"Correlation between and ischemic stroke is very common and not at least unusual. I present the case of a young patient who was first diagnosed with secondary erythrocytosis and after he developed an ischemic stroke more detailed diagnosis was made. He was then diagnosed with VHL c.571 C>G mutation (Croatian type). This case shows us the importance of scrutinizing cases, especially in very young patients.","PeriodicalId":93339,"journal":{"name":"MOJ clinical & medical case reports","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A case of a young patient diagnosed with the Hippel-Lindau disease c.571 C>G mutation (Croatian form) and multiple paragangliomas after developing ischemic stroke\",\"authors\":\"K. Blažina\",\"doi\":\"10.15406/MOJCR.2021.11.00373\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Correlation between and ischemic stroke is very common and not at least unusual. I present the case of a young patient who was first diagnosed with secondary erythrocytosis and after he developed an ischemic stroke more detailed diagnosis was made. He was then diagnosed with VHL c.571 C>G mutation (Croatian type). This case shows us the importance of scrutinizing cases, especially in very young patients.\",\"PeriodicalId\":93339,\"journal\":{\"name\":\"MOJ clinical & medical case reports\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"MOJ clinical & medical case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/MOJCR.2021.11.00373\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"MOJ clinical & medical case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/MOJCR.2021.11.00373","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A case of a young patient diagnosed with the Hippel-Lindau disease c.571 C>G mutation (Croatian form) and multiple paragangliomas after developing ischemic stroke
Correlation between and ischemic stroke is very common and not at least unusual. I present the case of a young patient who was first diagnosed with secondary erythrocytosis and after he developed an ischemic stroke more detailed diagnosis was made. He was then diagnosed with VHL c.571 C>G mutation (Croatian type). This case shows us the importance of scrutinizing cases, especially in very young patients.