Gaucher’s Disease

A. Rosenberg; N. Giladi

doi:10.1016/B978-0-12-374105-9.00326-9

Gaucher’s Disease

A. Rosenberg, N. Giladi

Clinical Departments

Tel Aviv University

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

Abstract

Gaucher’s disease (GD) is the most common lysosomal storage disease with a prevalence of 1 out of 75000 births and an even higher prevalence among Ashkenazi Jews. In the present overview, we will describe the pathological and clinical aspects as well as the treatment of the disease. Special attention will be paid to the recently described association between GD and Parkinson’s disease (PD).

Original language	English
Title of host publication	Encyclopedia of Movement Disorders, Three-Volume Set
Publisher	Elsevier
Pages	V1-531-V1-534
ISBN (Electronic)	9780123741059
DOIs	https://doi.org/10.1016/B978-0-12-374105-9.00326-9
State	Published - 1 Jan 2010

Keywords

Angiotensin-converting enzyme (ACE)
Bone marrow
Bone marrow transplants
Enzyme replacement therapy
Gaucher’s disease
Glucocerebrosidase
Glucocerebroside
Hepatomegaly
Lysosomal storage disease
Parkinsonism
Recombinant glucocerebrosidase
Splenectomy
Splenomegaly

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10.1016/B978-0-12-374105-9.00326-9

Cite this

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Gaucher’s Disease

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Keywords

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