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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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
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spelling doaj-51bdde6c02e5480789d1be7781f7167f2021-07-28T16:27:46ZrusLtd. “The National Academy of Pediatric Science and Innovation”Rossijskij Vestnik Perinatologii i Pediatrii1027-40652500-22282016-09-0161411412010.21508/1027-4065-2016-61-4-114-120346Skeletal system involvement in patients with mucopolysaccharidosis type IN. D. Vashakmadze0L. S. Namazova-Baranova1A. K. Gevorkyan2L. M. Kuzenkova3T. V. Podkletnova4M. A. Babaikina5A. V. Anikin6G. V. Kuznetsova7L. A. Osipova8Children’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowChildren’s Health Research Center, Ministry of Health of Russia, Moscow; N.I. Pirogov Russian National Research Medical University, Ministry of Health of Russia, MoscowJoint 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.https://www.ped-perinatology.ru/jour/article/view/363childrenmucopolysaccharidosis type iarticular syndromehip dysplasiadysostosismyelopathy
collection DOAJ
language Russian
format Article
sources DOAJ
author 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
spellingShingle 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
Skeletal system involvement in patients with mucopolysaccharidosis type I
Rossijskij Vestnik Perinatologii i Pediatrii
children
mucopolysaccharidosis type i
articular syndrome
hip dysplasia
dysostosis
myelopathy
author_facet 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
author_sort N. D. Vashakmadze
title Skeletal system involvement in patients with mucopolysaccharidosis type I
title_short Skeletal system involvement in patients with mucopolysaccharidosis type I
title_full Skeletal system involvement in patients with mucopolysaccharidosis type I
title_fullStr Skeletal system involvement in patients with mucopolysaccharidosis type I
title_full_unstemmed Skeletal system involvement in patients with mucopolysaccharidosis type I
title_sort skeletal system involvement in patients with mucopolysaccharidosis type i
publisher Ltd. “The National Academy of Pediatric Science and Innovation”
series Rossijskij Vestnik Perinatologii i Pediatrii
issn 1027-4065
2500-2228
publishDate 2016-09-01
description 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.
topic children
mucopolysaccharidosis type i
articular syndrome
hip dysplasia
dysostosis
myelopathy
url https://www.ped-perinatology.ru/jour/article/view/363
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