Skeletal system involvement in patients with mucopolysaccharidosis type I

Skeletal system involvement in patients with mucopolysaccharidosis type I

Joint pathology without signs of inflammation must always arouse suspicion of lysosomal storage diseases, mucopolysaccharidosis (MPS) in particular. It is these orthopedic diseases in mild MPS type I, which are an early sign of the disease; moreover, somatic disorders may be absent or present slight...

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Bibliographic Details
Main Authors: N. D. Vashakmadze, L. S. Namazova-Baranova, A. K. Gevorkyan, L. M. Kuzenkova, T. V. Podkletnova, M. A. Babaikina, A. V. Anikin, G. V. Kuznetsova, L. A. Osipova
Format: Article
Language:Russian
Published: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-09-01
Series:Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:
children
mucopolysaccharidosis type i
articular syndrome
hip dysplasia
dysostosis
myelopathy
Online Access:https://www.ped-perinatology.ru/jour/article/view/363
Description
Summary:Joint pathology without signs of inflammation must always arouse suspicion of lysosomal storage diseases, mucopolysaccharidosis (MPS) in particular. It is these orthopedic diseases in mild MPS type I, which are an early sign of the disease; moreover, somatic disorders may be absent or present slightly. Joint contractures are currently chosen as the starting point of an algorithm, a developed diagnostic algorithm for the examination of patients with MPS type I, which is also applicable to the early diagnosis of all forms of mild MPS.
ISSN:1027-4065
2500-2228

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