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

Juan Manuel Ortiz de Zárate, A. J. Rodríguez, C. Ortiz
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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.
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男性FATCO综合征(腓骨发育不全、胫骨campomelia和少指):病例报告
在多种出生缺陷中有腓骨发育不全,这是一种罕见的先天性频率,是一种低患病率综合征FATCO的一部分,腓骨发育不全(fibular aplasia),胫骨驼背(campomelia tibial)和少指畸形(oligosyndactyly)。我们报告了一个31个月大的男性病例,在哥伦比亚波哥大市一家康复院的礼貌和假肢咨询中进行了评估,他有FATCO综合征的病史和国外畸形的家族史。鉴于缺乏关于这种罕见综合征的报道和缺乏标准化的治疗方法,对假肢康复过程的评估很重要。
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