Abstract
Morquio syndrome is a rare genetic disorder caused by the lack of enzyme responsible for the breakdown of the mucopolysaccharide keratin sulphate which causes accumulation of glycosaminoglycans in various body tissues. Keeping in mind, this rare disease, we report two siblings from the same family with characteristics clinical as well as radiological features of this disorder.

Waqar Hussain . (2013) A Family with Mucopolysaccharidosis Type IV-Morquio Syndrome, , Volume 37, Issue 1.
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