Multidisciplinary Management of Hunter Syndrome-Reference-Cited by-同舟云学术

Multidisciplinary Management of Hunter Syndrome

Published:2009-12-01 Issue:6 Volume:124 Page:e1228-e1239
ISSN:0031-4005
Container-title:Pediatrics
language:en
Short-container-title:

Author:

Muenzer Joseph¹,Beck M.²,Eng C. M.³,Escolar M. L.¹,Giugliani R.⁴,Guffon N. H.⁵,Harmatz P.⁶,Kamin W.²,Kampmann C.²,Koseoglu S. T.⁶,Link B.⁷,Martin R. A.⁸,Molter D. W.⁹,Muñoz Rojas M. V.⁴,Ogilvie J. W.¹⁰,Parini R.¹¹,Ramaswami U.¹²,Scarpa M.¹³,Schwartz I. V.⁴,Wood R. E.¹⁴,Wraith E.¹⁵

Affiliation:

1. Department of Pediatrics, University of North Carolina, Chapel Hill, North Carolina

2. Villa Metabolica, Children's Hospital, University of Mainz, Mainz, Germany

3. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas

4. Medical Genetics Service, Hospital de Clinicas de Porto Alegre, and Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil

5. Hôpital Edouard Herriot Pavilion S, Maladies Metaboliques, Lyon, France

6. Division of Ophthalmology, Children's Hospital and Research Center Oakland, Oakland, California

7. Orthopedic Department, University Hospital Johannes Gutenberg-University, Mainz, Germany

8. Division of Medical Genetics, St Louis University, St Louis, Missouri

9. Department of Otolaryngology, Washington University in St Louis, St Louis, Missouri

10. Department of Orthopaedic Surgery, University of Utah School of Medicine, St Lake City, Utah

11. Pediatric Department, Ospedale San Gerardo, Monza, Italy

12. Paediatric Metabolic Unit, Addenbrooke's Hospital, Cambridge, United Kingdom

13. Department of Pediatrics, University of Padova, Padova, Italy

14. Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio

15. Inherited Metabolic Medicine, Genetic Medicine, St. Mary's Hospital, Manchester, United Kingdom

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Link

https://publications.aap.org/pediatrics/article-pdf/124/6/e1228/1022506/zpe012090e1228.pdf

Reference100 articles.

1. Neufeld EF, Muenzer J. The mucopolysaccharidoses. In: Scriver CR, ed. The Metabolic and Molecular Bases of Inherited Disease. New York, NY: McGraw-Hill; 2001:3421–3452

2. Bach G, Eisenberg F Jr, Cantz M, Neufeld EF. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci U S A. 1973;70(7):2134–2138

3. Martin R, Beck M, Eng C, et al. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics. 2008;121(2). Available at: www.pediatrics.org/cgi/content/full/121/2/e377

4. Young ID, Harper PS, Newcombe RG, Archer IM. A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms. J Med Genet. 1982;19(6):408–411

5. Vedolin L, Schwartz IV, Komlos M, et al. Correlation of MR imaging and MR spectroscopy findings with cognitive impairment in mucopolysaccharidosis II. AJNR Am J Neuroradiol. 2007;28(6):1029–1033

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