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Craniovertebral Abnormalities in Type VI Mucopolysaccharidosis (Maroteaux-Lamy Syndrome)

  • Published:2001-04-01 Issue:4 Volume:48 Page:849-853
  • ISSN:0148-396X
  • Container-title:Neurosurgery
  • language:en
  • Short-container-title:

Author:

Thorne John A.1,Javadpour Mohsen1,Hughes David G.2,Wraith Ed3,Cowie Richard A.1

Affiliation:

1. Department of Neurosurgery Royal Manchester Children's Hospital, Manchester, England

2. Department of Neuroradiology Royal Manchester Children's Hospital, Manchester, England

3. Department of Medicine Royal Manchester Children's Hospital, Manchester, England

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Surgery

Reference8 articles.

1. Otolaryngologic manifestations of the mucopolysaccharidoses;Bredenkamp;Ann Otol Rhinol Laryngol,1992

2. Bone marrow transplantation for Maroteaux-Lamy syndrome (MPS VI): Long-term follow-up;Herskhovits;J Inherit Metab Dis,1999

3. Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III;Krivit;Curr Opin Neurol,1999

4. A new dystosis with urinary excretion of chondroitin-sulphate B [in French];Maroteaux;Presse Med,1963

5. Occipito-atlanto-axial fusion in Morquio-Brailsford syndrome: A ten-year experience;Ransford,1996

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