Multidisciplinary management of arthrogryposis multiplex congenita type 2A case

Ranaivondrambola Tatiana, Randrianasolo Pascale, T. Servino, S. Duval
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Abstract

Arthrogryposis multiplex congenita (AMC) is a congenital disorder characterized by nonprogressive multiple joint contractures affecting one or more areas of the body, muscle weakness, and fibrosis. This term includes a heterogeneous group of diseases, neurological, neuromuscular, and genetic or mechanical origin. Two types of classification have been developed: A clinical one (types I, II, and III) and an etiological one. A multidisciplinary approach is needed for better care and appropriate follow-up. It is a case of AMC type 2A. A girl, with an antecedent of low levels of amniotic fluid, presented at birth with multiple malformations and stiffness of several articulations: bilateral clubfoot, bilateral clubhand, temporomandibular joint involvement, postural torticollis, and congenital hip dislocation. She had also a small persistence of arterial canal and ambiguous external genitalia. The care was performed by a multidisciplinary team including a physiatrist, pediatric surgeon, physiotherapist, prosthetist, and orthotist. In infants with arthrogryposis, joint stiffness is maximal at birth. The first step is passive mobilizations before surgical joint treatment. Azbell et al. found in their study that at 9 months of age, many of this infant's impairments of body structure and function, functional activity limitations, and participation restrictions improved. The program of stretching, muscle strengthening, facilitation of motor skills, orthopedic intervention, and parent education may have contributed to this infant's progress. Prospective intervention studies exploring specific intervention strategies are needed to establish the plan of care for these patients. Arthrogryposis describes a set of joint contractures present from birth and nonprogressive. The common physiopathological mechanism is fetal immobility syndrome. Multidisciplinary care is necessary and should be early and continued to gain maximum autonomy and facilitate social integration.
多发性先天性2A型关节挛缩症的多学科治疗
多发性先天性关节挛缩症(AMC)是一种先天性疾病,其特征是影响身体一个或多个部位的非进行性多发性关节挛缩、肌肉无力和纤维化。这个术语包括一组不同的疾病,有神经的、神经肌肉的、遗传的或机械的。目前已发展出两种类型的分类:临床分类(I、II和III型)和病因分类。需要多学科的方法来提供更好的护理和适当的随访。这是一例AMC 2A型病例。女婴,羊水水平低,出生时出现多种畸形和多个关节僵硬:双侧畸形足、双侧畸形手、颞下颌关节受累、体位性斜颈和先天性髋关节脱位。她也有小的动脉管和模糊的外生殖器。该护理由一个多学科团队完成,包括物理医生、儿科外科医生、物理治疗师、假肢医生和矫形师。在关节挛缩的婴儿中,关节僵硬在出生时是最大的。第一步是关节手术治疗前的被动活动。Azbell等人在他们的研究中发现,在9个月大时,婴儿的许多身体结构和功能障碍、功能活动限制和参与限制得到改善。伸展、肌肉强化、促进运动技能、矫形干预和父母教育可能有助于婴儿的进步。需要前瞻性干预研究,探索具体的干预策略,为这些患者制定护理计划。关节挛缩症是指一组从出生开始就存在的关节挛缩,且不进行性。常见的生理病理机制是胎儿不动综合征。多学科护理是必要的,应该尽早进行,并继续获得最大的自主权,促进社会融合。
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