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Practical management of behavioral problems in mucopolysaccharidoses disorders.

Authors :
Escolar, Maria L.
Jones, Simon A.
Shapiro, Elsa G.
Horovitz, Dafne D.G.
Lampe, Christina
Amartino, Hernán
Source :
Molecular Genetics & Metabolism. Dec2017 Supplement, Vol. 122, p35-40. 6p.
Publication Year :
2017

Abstract

The mucopolysaccharidosis (MPS) disorders are caused by deficiencies of specific lysosomal enzymes, resulting in progressive glycosaminoglycan (GAG) accumulation in cells and tissues throughout the body. Excessive GAG storage can lead to a variety of somatic manifestations as well as primary and secondary neurological symptoms. Behavioral problems (like hyperactivity, attention difficulties, and severe frustration) and sleeping problems are typical primary neurological symptoms of MPS caused by GAG accumulation in neurons, and are frequently observed in patients with MPS I, II, III, and VII. As these problems often place a significant burden on the family, proper management is important. This review summarizes current insights into behavioral and sleeping problems in MPS disorders and the most optimal management approaches, as presented and discussed during a meeting of an international group of experts with extensive experience in managing and treating MPS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10967192
Volume :
122
Database :
Academic Search Index
Journal :
Molecular Genetics & Metabolism
Publication Type :
Academic Journal
Accession number :
126947041
Full Text :
https://doi.org/10.1016/j.ymgme.2017.09.010