[ 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
ELEMENTARY SCHOOL PUNCTUATION QUIZ
Punctuation marks help make writing easy to read and understand. Some of the most important ones are the period (.), comma (,), question mark (?), and exclamation point (!). How well do you know how to use them? Find out in this quiz!
Question 1 of 10
Which punctuation mark is best for this sentence? "Can I watch a movie __"
The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.