|
|
|
|
Definition: |
A gel-like substance found in body cells, mucous secretions, and synovial fluids.
|
Information: |
When there is a deficiency of enzymes necessary to breakdown mucopolysaccharides, a condition called mucopolysaccharidosis (MPS) exists. Mucopolysaccharidoses are a group of genetic disorders that result in excessive accumulation of mucopolysaccharides in body tissues and results in many serious physical disorders.
Usually, this results in various genetic deformities such as skeletal deformities (especially of the face), mental retardation, and decreased life expectancy. Examples of these disorders are: Hunter syndrome, Hurler syndrome, Scheie syndrome, Sanfilippo syndrome, Maroteaux-Lamy syndrome, and Morquio disease.
|
|
|
Review Date: 1/4/2002
Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.
|
|
A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is the first of its kind, requiring compliance with 53 standards of quality and accountability, verified by independent audit. A.D.A.M. is among the first to achieve this important distinction for online health information and services. A.D.A.M. is also a founding member of Hi-Ethics (www.hiethics.com) and subscribes to the principles of the Health on the Net Foundation (www.hon.ch).
|
The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2003 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.
|