Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux–Lamy syndrome): under-recognized and challenging to diagnose-Reference-Cited by-同舟云学术

Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux–Lamy syndrome): under-recognized and challenging to diagnose

Published:2014-01-04 Issue:3 Volume:43 Page:359-369
ISSN:0364-2348
Container-title:Skeletal Radiology
language:en
Short-container-title:Skeletal Radiol

Author:

Lachman Ralph S.,Burton Barbara K.,Clarke Lorne A.,Hoffinger Scott,Ikegawa Shiro,Jin Dong-Kyu,Kano Hiroki,Kim Ok-Hwa,Lampe Christina,Mendelsohn Nancy J.,Shediac Renée,Tanpaiboon Pranoot,White Klane K.

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging

Link

http://link.springer.com/article/10.1007/s00256-013-1797-y/fulltext.html

Reference20 articles.

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2. Warman ML, Cormier-Daire V, Hall C, Krakow D, Lachman R, LeMerrer M, et al. Nosology and classification of genetic skeletal disorders: 2010 revision. Am J Med Genet A. 2011;155A(5):943–68.

3. Valayannopoulos V, Wijburg FA. Therapy for the mucopolysaccharidoses. Rheumatology (Oxford). 2011;50 Suppl 5:v49–59.

4. Wood TC, Harvey K, Beck M, Burin MG, Chien YH, Church HJ, et al. Diagnosing mucopolysaccharidosis IVA. J Inherit Metab Dis. 2013;36(2):293–307.

5. Wood T, Bodamer OA, Burin MG, D'Almeida V, Fietz M, Giugliani R, et al. Expert recommendations for the laboratory diagnosis of MPS VI. Mol Genet Metab. 2012;106(1):73–82.

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