Oral and craniofacial manifestations of mucopolysaccharidoses
Mucopolysaccharidoses (MPS) are a group of inherited metabolic disorders caused by the deficiency of lysosomal enzymes necessary for the degradation of glycosaminoglycans (GAGs). Non-degraded GAGs accumulate inside the lysosomes and compromise cell function in different tissues and organs. This accu...
Main Author: | |
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Other Authors: | , |
Format: | article |
Language: | eng |
Published: |
2020
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Subjects: | |
Online Access: | http://hdl.handle.net/10284/8992 |
Country: | Portugal |
Oai: | oai:bdigital.ufp.pt:10284/8992 |