Musculoskeletal anomalies in children with mucopolysaccaridoses

Автор: Mller Florence, Alomar Khaled, Journeau Pierre

Журнал: Гений ортопедии @geniy-ortopedii

Рубрика: Оригинальные статьи

Статья в выпуске: 4 т.27, 2021 года.

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Introduction The accumulation of glycosaminoglycan (GAGs) in the tissues in Mucopolysaccharidoses (MPS) can lead to skeletal anomalies (DYSOSTOSIS MULTIPLEX) and to soft tissue impairments (neural or medullar compression, joint stiffness, tenosynovitis). Here is a review of orthopedic issues frequently encountered in patients with MPS. Material and methods Surgery may be justified at different age and according to the type of MPS. Different surgical approaches and their indications are exposed in the article. Results The article exposes indications and techniques for orthopedic issues in MPS children: cervical stenosis, cervical instability, kyphosis, hip dysplasia and hip dislocation, genu valgum. Conclusion Various musculoskeletal anomalies can be found in patients with mucopolysaccharidoses. Neurological impairments are frequently seen due to cervical stenosis or instability and should be early detected with regular MRI of the cervical spine. Well-codified management should lead to favorable functional results and maintain functional and walking abilities.

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Mucopolysaccharidoses, musculoskeletal anomalies, orthopedic surgery

Короткий адрес: https://sciup.org/142229730

IDR: 142229730   |   DOI: 10.18019/1028-4427-2021-27-4-446-449

Список литературы Musculoskeletal anomalies in children with mucopolysaccaridoses

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