Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data

Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data

Abstract Background Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder caused by deficiency in acid beta-glucosidase. GD exhibits a wide clinical spectrum of disease severity with an unpredictable natural course. Plasma chitotriosidase activity and CC chemokine ligand 18 (CCL1...

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Bibliographic Details
Main Authors: Tatiana Raskovalova, Patrick B. Deegan, Ruby Yang, Elena Pavlova, Jérome Stirnemann, José Labarère, Ari Zimran, Pramod K. Mistry, Marc Berger
Format: Article
Language:English
Published: BMC 2017-04-01
Series:Systematic Reviews
Subjects:
Gaucher disease
Biomarkers
Chemokines, CC
Hexosaminidases
Hepatomegaly
Splenomegaly
Online Access:http://link.springer.com/article/10.1186/s13643-017-0483-x

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http://link.springer.com/article/10.1186/s13643-017-0483-x

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