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Published in: Journal of Inherited Metabolic Disease 5/2011

01-10-2011 | Original Article

Four-year follow-up of chronic neuronopathic Gaucher disease in Europeans using a modified severity scoring tool

Authors: Elin Haf Davies, Eugen Mengel, Anna Tylki-Szymanska, G. Kleinotiene, Joerg Reinke, Ashok Vellodi

Published in: Journal of Inherited Metabolic Disease | Issue 5/2011

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Abstract

In 2007, the European Task Force for neuronopathic Gaucher disease (NGD) published a review of 55 patients across four countries. Although some observations were possible, analysis was difficult due to the absence of a systematic way of assessing patients. In response to this, a Severity Scoring Tool (SST) was devised to offer a systematic means of assessing the neurological presentation seen. The SST has been modified (mSST) and is a valid tool for monitoring neurological progression. This review describes disease status and progression of neurological manifestations in a cohort of 39 chronic NGD patients across three European countries over a period of 4 years, using the mSST.
Literature
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go back to reference Schiffmann R, Fitzgibbon EJ, Harris C, DeVile C, Davies EH, Abel L, van Schaik I, Timmons M, Ries M, Vellodi A (2008) A randomized controlled trial of miglustat in Gaucher disease type 3. Ann Neurol 64(5):514–22PubMedCrossRef Schiffmann R, Fitzgibbon EJ, Harris C, DeVile C, Davies EH, Abel L, van Schaik I, Timmons M, Ries M, Vellodi A (2008) A randomized controlled trial of miglustat in Gaucher disease type 3. Ann Neurol 64(5):514–22PubMedCrossRef
go back to reference Tylki-Szymańska A, Vellodi A, El-Beshlawy A, Cole JA, Kolodny E (2010) Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes Subregistry. J Inherit Metab Dis 33(4):339–46PubMedCrossRef Tylki-Szymańska A, Vellodi A, El-Beshlawy A, Cole JA, Kolodny E (2010) Neuronopathic Gaucher disease: demographic and clinical features of 131 patients enrolled in the International Collaborative Gaucher Group Neurological Outcomes Subregistry. J Inherit Metab Dis 33(4):339–46PubMedCrossRef
go back to reference Vellodi A, Bembi B, de Villemeur TB, Collin-Histed T, Erikson A, Mengel E, Rolfs A, Tylki-Szymanska A (2001) Neuronopathic Gaucher Disease Task Force of the European Working Group on Gaucher Disease. 2001 Management of neuronopathic Gaucher disease: a European consensus. J Inherit Metab Dis 24(3):319–27PubMedCrossRef Vellodi A, Bembi B, de Villemeur TB, Collin-Histed T, Erikson A, Mengel E, Rolfs A, Tylki-Szymanska A (2001) Neuronopathic Gaucher Disease Task Force of the European Working Group on Gaucher Disease. 2001 Management of neuronopathic Gaucher disease: a European consensus. J Inherit Metab Dis 24(3):319–27PubMedCrossRef
go back to reference Vellodi A, Tylki-Szymanska A, Davies EH, Kolodny E, Bembi B, Collin-Histed T, Mengel E, Erikson A, Schiffmann R (2009) Management of neuronopathic Gaucher disease: revised recommendations. J Inherit Metab Dis 32(5):660–4, Aug 5PubMedCrossRef Vellodi A, Tylki-Szymanska A, Davies EH, Kolodny E, Bembi B, Collin-Histed T, Mengel E, Erikson A, Schiffmann R (2009) Management of neuronopathic Gaucher disease: revised recommendations. J Inherit Metab Dis 32(5):660–4, Aug 5PubMedCrossRef
Metadata
Title
Four-year follow-up of chronic neuronopathic Gaucher disease in Europeans using a modified severity scoring tool
Authors
Elin Haf Davies
Eugen Mengel
Anna Tylki-Szymanska
G. Kleinotiene
Joerg Reinke
Ashok Vellodi
Publication date
01-10-2011
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 5/2011
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-011-9347-z

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