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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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Russo
Argitaratua: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-09-01
Saila:Rossijskij Vestnik Perinatologii i Pediatrii
Gaiak:
Sarrera elektronikoa:https://www.ped-perinatology.ru/jour/article/view/363
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