Abstract
Mucopolysaccharidosis (MPS) refers to a group of genetic disorder characterized by excessive accumulation of mucopolysaccharides secondary to deficiencies in specific enzymes. It produces characteristic skeletal abnormalities collectively termed as “dysostosis multiplex”. Here we describe a young female child with classical radiological features of MPS on plain radiographs. JMS 2012;15(1):54-56.
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CITATION STYLE
APA
Wani, A. I., Farooqi, K. J., Bashir, M. I., Mir, S. A., & Masoodi, S. R. (2012). Mucopolysaccharidosis: Clinical and Radiological Aspects. JMS SKIMS, 15(1), 54–56. https://doi.org/10.33883/jms.v15i1.115
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