Síndrome de FATCO (aplasia fibular, campomelia de tibia y oligosindactilia) en paciente masculino: reporte de caso

Autor:	Andrea J. Rodríguez, Juan Manuel Guevara Zarate, Carlos A. Ortiz
Rok vydání:	2018
Předmět:	musculoskeletal diseases medicine.medical_specialty business.industry Fatco Syndrome Prosthetic rehabilitation medicine.medical_treatment Oligosyndactyly Fibular aplasia musculoskeletal system Prosthesis Surgery Medicine Rare syndrome Tibia Family history business
Zdroj:	Revista Colombiana de Médicina Física y Rehabilitación. 28:70-74
ISSN:	2256-5655 0121-0041
DOI:	10.28957/rcmfr.v28n1a7
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::90c51090891ad6cb9e9bb8ef98672990 https://doi.org/10.28957/rcmfr.v28n1a7 Zobrazit plný text záznamu