Jordan Killingsworth, Evan Abdullah, Ikram Rostane, Shreeya Patel, Colin Jenkins, Brittany Graham, Rajesh Pandey, Matthew Greives
{"title":"在一名新生儿身上孤立地发现疟原虫","authors":"Jordan Killingsworth, Evan Abdullah, Ikram Rostane, Shreeya Patel, Colin Jenkins, Brittany Graham, Rajesh Pandey, Matthew Greives","doi":"10.1177/27325016241254507","DOIUrl":null,"url":null,"abstract":"Acalvaria is a rare congenital malformation of unknown etiopathogenesis that affects the development of the skull and surrounding muscular structures. There is scant literature regarding the pathophysiology, and no standardized guidelines exist for patient management. Herein, we present a case of acalvaria in a newborn and our multidisciplinary approach from diagnosis to 1 year of age.","PeriodicalId":508736,"journal":{"name":"FACE","volume":" 476","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolated Finding of Acalvaria in a Newborn Infant\",\"authors\":\"Jordan Killingsworth, Evan Abdullah, Ikram Rostane, Shreeya Patel, Colin Jenkins, Brittany Graham, Rajesh Pandey, Matthew Greives\",\"doi\":\"10.1177/27325016241254507\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Acalvaria is a rare congenital malformation of unknown etiopathogenesis that affects the development of the skull and surrounding muscular structures. There is scant literature regarding the pathophysiology, and no standardized guidelines exist for patient management. Herein, we present a case of acalvaria in a newborn and our multidisciplinary approach from diagnosis to 1 year of age.\",\"PeriodicalId\":508736,\"journal\":{\"name\":\"FACE\",\"volume\":\" 476\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FACE\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/27325016241254507\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FACE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/27325016241254507","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Acalvaria is a rare congenital malformation of unknown etiopathogenesis that affects the development of the skull and surrounding muscular structures. There is scant literature regarding the pathophysiology, and no standardized guidelines exist for patient management. Herein, we present a case of acalvaria in a newborn and our multidisciplinary approach from diagnosis to 1 year of age.
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