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

• Main Authors: Natalia V. Buchinskaya (Author), Mikhail M. Kostik (Author), Oksana L. Kolobova (Author), Larisa N. Melnikova (Author)
• Formato: Libro
• Publicado: "Paediatrician" Publishers LLC, 2019-01-01T00:00:00Z.
• Subjects: article
• Acceso en liña: Connect to this object online.

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...