{"title":"诊断Peutz-Jeghers综合征的临床标准:寻找缺失的东西","authors":"","doi":"10.32512/jmr.3.3.2020/22.23","DOIUrl":null,"url":null,"abstract":"The Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by\nhamartomatous gastrointestinal polyposis and mucocutaneous melanin pigmentation. In\nthis report we discuss diagnostic circumstances of new PJS family.\nKeywords:\nIntestinal obstruction; intussusception; Peutz-Jeghers syndrome; polyps; surgery.","PeriodicalId":354267,"journal":{"name":"JUNIOR MEDICAL RESEARCH","volume":"92 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical criteria for Peutz-Jeghers syndrome diagnosis: Look for what is missing\",\"authors\":\"\",\"doi\":\"10.32512/jmr.3.3.2020/22.23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by\\nhamartomatous gastrointestinal polyposis and mucocutaneous melanin pigmentation. In\\nthis report we discuss diagnostic circumstances of new PJS family.\\nKeywords:\\nIntestinal obstruction; intussusception; Peutz-Jeghers syndrome; polyps; surgery.\",\"PeriodicalId\":354267,\"journal\":{\"name\":\"JUNIOR MEDICAL RESEARCH\",\"volume\":\"92 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JUNIOR MEDICAL RESEARCH\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32512/jmr.3.3.2020/22.23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JUNIOR MEDICAL RESEARCH","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32512/jmr.3.3.2020/22.23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Clinical criteria for Peutz-Jeghers syndrome diagnosis: Look for what is missing
The Peutz-Jeghers syndrome (PJS) is an autosomal dominant disorder characterized by
hamartomatous gastrointestinal polyposis and mucocutaneous melanin pigmentation. In
this report we discuss diagnostic circumstances of new PJS family.
Keywords:
Intestinal obstruction; intussusception; Peutz-Jeghers syndrome; polyps; surgery.
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