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

• Κύριοι συγγραφείς: Natalia V. Buchinskaya (Συγγραφέας), Mikhail M. Kostik (Συγγραφέας), Oksana L. Kolobova (Συγγραφέας), Larisa N. Melnikova (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: "Paediatrician" Publishers LLC, 2019-01-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: 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...