THE MANAGEMENT OF PATIENTS WITH GAUCHER DISEASE, TYPE 1

THE MANAGEMENT OF PATIENTS WITH GAUCHER DISEASE, TYPE 1

<p>Background. Accumulation of glucocerebroside in spleen, liver, bone marrow and bones, but rarely in other organs, due to inborn deficiency of lisosomal enzyme glucocerebrosidase leads to Gaucher disease. The most common is type 1, chronic non-neuronopathic form of Gaucher disease. In type 1...

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Bibliographic Details
Main Authors: Majda Benedik-Dolničar, Lidija Kitanovski
Format: Article
Language:English
Published: Slovenian Medical Association 2003-12-01
Series:Zdravniški Vestnik
Subjects:
Gaucher
guidelines
management
diagnostic
treatment
Online Access:http://vestnik.szd.si/index.php/ZdravVest/article/view/1895

Internet

http://vestnik.szd.si/index.php/ZdravVest/article/view/1895

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