[ hûr′lərz ]
A hereditary defect in mucopolysaccharide metabolism characterized by the excretion of dermatan sulfate and heparitin sulfate in the urine, abnormal development of skeletal cartilage and bone, corneal clouding, enlarged liver and spleen, mental retardation and sometimes deafness, and a coarsened facial surface with flattened nose and enlarged lips.dysostosis multiplex Hurler's disease lipochondrodystrophy type I mucopolysaccharidosis
What’s The #’s Real Name?How do we currently use the # symbol? On Twitter, Facebook, and Instagram, you tag your friends with the @ symbol and you tag topics with the #. If you see something that says “#WordoftheDay,” the tweet or post has something to do with Word of the Day. And, once you click on that marked topic, you’ll likely see all public posts about it. It’s a …
The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.