How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease?

How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease?

Mucopolysaccharidosis type I (MPS I) is a hereditary metabolic disease that manifests itself in childhood by systemic damage to tissues and organs, a constantly progressive course leading to disability. Diagnosis of mild forms of the disease is particularly difficult due to the absence of specific s...

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Bibliographic Details
Main Authors: Natalia V. Buchinskaya, Mikhail M. Kostik, Oksana L. Kolobova, Larisa N. Melnikova
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2019-01-01
Series:Вопросы современной педиатрии
Subjects:
children
mucopolysaccharidosis type i
mps
stiffness
dry arthritis
algorithm
diagnosis
Online Access:https://vsp.spr-journal.ru/jour/article/view/1979
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