| Literature DB >> 12611487 |
Judit Várkonyi1, Zsuzsa Simon, Krisztina Soós, Anna Poros.
Abstract
Gaucher disease type I is the so-called non-neuronal adult form of the autosomally inherited lysosomal storage disease. The simultaneous occurrence of Gaucher disease with Parkinson's syndrome has been reported to aggravate both disorders, leading to an unusually early onset and therapy resistance. Neurological alterations in Gaucher disease type I are mostly related to CNS bleeding and skeletal complications. The patient presented here was sensitive to combination therapy for 5 years.Entities:
Mesh:
Year: 2002 PMID: 12611487 DOI: 10.1163/15685590260461084
Source DB: PubMed Journal: Haematologia (Budap) ISSN: 0017-6559