Congenital hyperextension deformity of the knees due to arthrogryposis multiplex congenita? Case report

Paola Andrea Romero-Campiño, Liliana Sandoval-Tristancho, M. C. Jaramillo, Anna Claici, L. P. Montaña-Jiménez
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Abstract

Introduction: Arthrogryposis multiplex congenita is a disorder characterized by non-progressive joint contractures. It has an estimated prevalence of 1 in every 3 000-5 000 live births, with the same male-to-female ratio.Case presentation: This is the case of a male newborn with adequate prenatal care checkup appointments, who presented with a congenital deformity of the lower limbs. On physical examination, he had hyperextension of the knees (passive flexion of 20° in the left leg and 30° in the right leg), and painful active movement. On admission, peripheral pulses had good intensity, and adequate distal perfusion was found. Barlow and Ortolani maneuvers were negative, and no midline lesions were observed in the spine. The patient was diagnosed with arthrogryposis multiplex congenita and received multidisciplinary treatment to avoid early morbidity and mortality.Conclusion: To attain satisfactory clinical development in patients with arthrogryposis, it is essential to have a high level of antenatal suspicion, as well as appropriate prenatal checkups. All this allows for proper management, minimizing diagnostic errors, avoiding unnecessary procedures, and performing effective and timely treatment with outstanding results.
多重先天性关节挛缩导致的先天性膝关节过伸畸形?病例报告
简介:先天性多发性关节挛缩是一种以非进行性关节挛缩为特征的疾病。估计患病率为每3 000-5 000例活产中有1例,男女比例相同。病例介绍:这是一个男婴与充分的产前护理检查预约,谁提出了先天性畸形的下肢。体检时,患者膝关节过伸(左腿被动屈曲20°,右腿被动屈曲30°),主动活动时疼痛。入院时外周脉搏强度良好,远端灌注充足。Barlow和Ortolani手法阴性,脊柱未见中线病变。患者被诊断为先天性多发性关节挛缩,并接受多学科治疗,以避免早期发病和死亡。结论:要使关节挛缩症患者获得满意的临床发展,必须有高度的产前怀疑,并进行适当的产前检查。所有这些都允许适当的管理,最大限度地减少诊断错误,避免不必要的程序,并进行有效和及时的治疗,并取得出色的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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