Publication Type : Journal Article
Publisher : National Journal of Physiology, Pharmacy and Pharmacology.
Source : National Journal of Physiology, Pharmacy and Pharmacology, vol. 7, no. 10, pp. 1137-1138, 2017.
Campus : Kochi
School : School of Pharmacy
Department : Pharmacy Practice
Verified : No
Year : 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., Roshni P. R., and Kumar, N. M., “A case report on Winchester syndrome”, National Journal of Physiology, Pharmacy and Pharmacology, vol. 7, no. 10, pp. 1137-1138, 2017.