Publication Type:

Journal Article

Source:

1992, Volume 74 (2017)

Abstract:

The mucopolysaccharidoses are a group of inherited lysosomal storage diseases that are caused by a deficiency of specific enzymes. The acid mucopolysaccharides are stored in tissue and excreted in large quantities in the urine. The storage of this material leads to effects on a wide variety of tissues and to remarkable changes in morphologic features. Winchester syndrome is a rare disorder in the group of mucopolysaccharidoses. This article is a report of a case with classic clinical, radiologic, and biochemical characteristics of the Winchester syndrome.

Cite this Research Publication

M. Mathew, Thomas, P., Kumar, N. M., and Roshni P. R., “Winchester syndrome: A case report and literature review”, 1992, vol. 74, 2017.

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