Maroteaux-Lamy syndrome–mucopolysaccharidosis type VI: a case report (errors and complications)

Abstract

The authors present a case of mucopolysaccharidosis type VI in a child. Low incidence rate of mucopolysaccharidosis in pediatric population, its difficult differential diagnosis and treatment suggests that this description of the disease pathology and treatment with the analysis of errors and complications in an 11-year-old child would be of interest for orthopedists, neurologists, anesthesiologists, and pediatricians.