Morquio-B syndrome (MPS-IV B) associated with β-galactosidase deficiency in two siblings

Author:

Sheth Jayesh J.,Sheth Frenny J.,Bhattacharya Raktima

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Mckusick VA.Heritable Disorders of Connective Tissue. 4th edn, St. Louis: Mosby; 1972.

2. Matalon R, Arbogast B, Justice P, Brandt P, Brandt Ek, Dorfman A. Morquio’s syndrome. Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase.Biochem Biophys Res Commun 1974; 61: 759.

3. Groebe H, Krins M, Schmidberger H, Von Figura K, Harzer Ket al. MPS IV B associated with β-galactosidase deficiency. Report of two cases.Am J Hum Genet 1980; 32: 258.

4. Van der Horst GTJ, Kleijer WJ, Hoogeveen AT, Huijmans JGM, Blom W, Van Diggelen OP. Morquio B syndrome: A primary defect in β-galactosidase.Am J Med Genet 1983; 16: 261.

5. Beck M, Pefersen EM, Spranger J, Brighton P. Morquio’s disease type B (β-galactosidase deficiency) in three siblings.Afr Med J 1987; 72: 704.

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