Bilateral anterior cruciate ligament agenesis in a 12-year-old boy: A rare case report.

IF 1
Eren Akın, Salih Kagan Kurun, Lokman Kehribar, Ahmet Emin Okutan
{"title":"Bilateral anterior cruciate ligament agenesis in a 12-year-old boy: A rare case report.","authors":"Eren Akın, Salih Kagan Kurun, Lokman Kehribar, Ahmet Emin Okutan","doi":"10.5152/j.aott.2026.25787","DOIUrl":null,"url":null,"abstract":"<p><p>Bilateral anterior cruciate ligament (ACL) agenesis is an exceptionally rare condition. Only a limited number of bilateral ACL agenesis cases have been reported in the literature, and these patients typically present with additional congenital anomalies or other pathologies involving the knee joint. Here, a 12-year-old male patient was reported with bilateral absence of the ACL, who had no comorbidities other than a history of casting and Achilles tenoplasty performed for pes equinovarus. The patient presented to the clinic with bilateral knee laxity and a sense of instability during daily activities. Magnetic resonance imaging of both knees revealed bilateral ACL agenesis. Unlike most previously published cases, the patient had no associated congenital anomalies or accompanying pathologies, making this case a rare example in the existing literature.   Cite this article as: Akin E, Kurun SK, Kehribar L, Okutan AE. Bilateral anterior cruciate ligament agenesis in a 12-year-old boy: A rare case report. Acta Orthop Traumatol Turc., 2026; 60(4), 0787, . doi: 10.5152/j.aott.2026.25787.</p>","PeriodicalId":93854,"journal":{"name":"Acta orthopaedica et traumatologica turcica","volume":"60 4","pages":""},"PeriodicalIF":1.0000,"publicationDate":"2026-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13507782/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta orthopaedica et traumatologica turcica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5152/j.aott.2026.25787","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Bilateral anterior cruciate ligament (ACL) agenesis is an exceptionally rare condition. Only a limited number of bilateral ACL agenesis cases have been reported in the literature, and these patients typically present with additional congenital anomalies or other pathologies involving the knee joint. Here, a 12-year-old male patient was reported with bilateral absence of the ACL, who had no comorbidities other than a history of casting and Achilles tenoplasty performed for pes equinovarus. The patient presented to the clinic with bilateral knee laxity and a sense of instability during daily activities. Magnetic resonance imaging of both knees revealed bilateral ACL agenesis. Unlike most previously published cases, the patient had no associated congenital anomalies or accompanying pathologies, making this case a rare example in the existing literature.   Cite this article as: Akin E, Kurun SK, Kehribar L, Okutan AE. Bilateral anterior cruciate ligament agenesis in a 12-year-old boy: A rare case report. Acta Orthop Traumatol Turc., 2026; 60(4), 0787, . doi: 10.5152/j.aott.2026.25787.

12岁男孩双侧前交叉韧带发育不全:罕见病例报告。
双侧前交叉韧带(ACL)发育不全是一种非常罕见的疾病。文献中仅报道了数量有限的双侧前交叉韧带不全病例,这些患者通常伴有额外的先天性异常或涉及膝关节的其他病变。本文报道一名12岁男性患者,双侧前交叉韧带缺失,除有马蹄内翻铸造和跟腱成形术史外,无其他合并症。患者就诊时双侧膝关节松弛,日常活动时感觉不稳定。双膝磁共振成像显示双侧ACL发育不全。与大多数先前发表的病例不同,该患者没有相关的先天性异常或伴随的病理,使该病例在现有文献中罕见。引用本文为:Akin E, Kurun SK, Kehribar L, Okutan AE。12岁男孩双侧前交叉韧带发育不全:罕见病例报告。骨科创伤学报。, 2026;60(4), 0787,。doi: 10.5152 / j.aott.2026.25787。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书