{"title":"科斯特洛综合征","authors":"B. Kerr, K. Gripp, E. Wright","doi":"10.1002/0471695998.mgs014","DOIUrl":null,"url":null,"abstract":"In 1971, Costello described a new syndrome in 2 patients. The major clinical findings comprise short stature; redundant skin of the neck, palms, soles, and fingers; curly hair; relative macrocephaly; depressed nasal bridge; papillomata around the mouth and nares; distinct facial gestalt; hyperextensible joints; and mental retardation. We present a third patient and review the manifestations of this condition.","PeriodicalId":142022,"journal":{"name":"Cassidy and Allanson's Management of Genetic Syndromes","volume":"24 1","pages":"69-73"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"98","resultStr":"{\"title\":\"COSTELLO SYNDROME\",\"authors\":\"B. Kerr, K. Gripp, E. Wright\",\"doi\":\"10.1002/0471695998.mgs014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In 1971, Costello described a new syndrome in 2 patients. The major clinical findings comprise short stature; redundant skin of the neck, palms, soles, and fingers; curly hair; relative macrocephaly; depressed nasal bridge; papillomata around the mouth and nares; distinct facial gestalt; hyperextensible joints; and mental retardation. We present a third patient and review the manifestations of this condition.\",\"PeriodicalId\":142022,\"journal\":{\"name\":\"Cassidy and Allanson's Management of Genetic Syndromes\",\"volume\":\"24 1\",\"pages\":\"69-73\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"98\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cassidy and Allanson's Management of Genetic Syndromes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/0471695998.mgs014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cassidy and Allanson's Management of Genetic Syndromes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471695998.mgs014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
In 1971, Costello described a new syndrome in 2 patients. The major clinical findings comprise short stature; redundant skin of the neck, palms, soles, and fingers; curly hair; relative macrocephaly; depressed nasal bridge; papillomata around the mouth and nares; distinct facial gestalt; hyperextensible joints; and mental retardation. We present a third patient and review the manifestations of this condition.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
