Juan Manuel Ortiz de Zárate, A. J. Rodríguez, C. Ortiz
{"title":"Síndrome de FATCO (aplasia fibular, campomelia de tibia y oligosindactilia) en paciente masculino: reporte de caso","authors":"Juan Manuel Ortiz de Zárate, A. J. Rodríguez, C. Ortiz","doi":"10.28957/RCMFR.V28N1A7","DOIUrl":null,"url":null,"abstract":"Among the multiple birth defects is fibular aplasia, which is a rare congenital frequency that is part of a low prevalence syndrome called FATCO, fibular aplasia (fibular aplasia), campomelia of the tibia (Campomelia tibial) and oligosyndactyly (Oligosyndactyly). We present the case of a male man of 31 months of age evaluated in the courtesy and prosthesis consultation in a rehabilitation house in the city of Bogota, Colombia, with a history of FATCO syndrome and the family history of malformations abroad. Given the paucity of reports on this rare syndrome and the lack of a standardized treatment approach, evaluation of the prosthetic rehabilitation process is important.","PeriodicalId":329310,"journal":{"name":"Revista Colombiana de Médicina Física y Rehabilitación","volume":"119 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Colombiana de Médicina Física y Rehabilitación","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.28957/RCMFR.V28N1A7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Among the multiple birth defects is fibular aplasia, which is a rare congenital frequency that is part of a low prevalence syndrome called FATCO, fibular aplasia (fibular aplasia), campomelia of the tibia (Campomelia tibial) and oligosyndactyly (Oligosyndactyly). We present the case of a male man of 31 months of age evaluated in the courtesy and prosthesis consultation in a rehabilitation house in the city of Bogota, Colombia, with a history of FATCO syndrome and the family history of malformations abroad. Given the paucity of reports on this rare syndrome and the lack of a standardized treatment approach, evaluation of the prosthetic rehabilitation process is important.