Mucopolysaccharidosis in children type Ⅳ

Mucopolysaccharidosis in children type Ⅳ, also known as mucopolysaccharidosis type; Mucopolysaccharidosis type; Mucopolysaccharidosis type; Golberger syndrome; β-glucosidase deficiency; Goldberg syndrome . Recessive for autosomal. Its clinical features are extensive bone lesions other than the skull and face bones. At the beginning of the 20th century (Thompson, 1900), mucopolysaccharidosis has been recorded. Hurler and Pfaundler (1919) respectively reported the type of short trunk and skeletal deformity in children with mental retardation. Mucopolysaccharidosis type IV was first reported by Morquio and Breilsford in Uruguay in 1929.

The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments.