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dc.contributor.author
Dardis, A.  
dc.contributor.author
Michelakakis, H.  
dc.contributor.author
Rozenfeld, Paula Adriana  
dc.contributor.author
Fumic, K.  
dc.contributor.author
Wagner, J.  
dc.contributor.author
Pavan, E.  
dc.contributor.author
Fuller, M.  
dc.contributor.author
Revel Vilk, S.  
dc.contributor.author
Hughes, D.  
dc.contributor.author
Cox, T.  
dc.contributor.author
Aerts, J.  
dc.date.available
2023-09-26T09:54:59Z  
dc.date.issued
2022-10  
dc.identifier.citation
Dardis, A.; Michelakakis, H.; Rozenfeld, Paula Adriana; Fumic, K.; Wagner, J.; et al.; Patient centered guidelines for the laboratory diagnosis of Gaucher disease type 1; BioMed Central; Orphanet Journal Of Rare Diseases; 17; 1; 10-2022; 1-17  
dc.identifier.issn
1750-1172  
dc.identifier.uri
http://hdl.handle.net/11336/212997  
dc.description.abstract
Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder due to the deficient activity of the acid beta-glucosidase (GCase) enzyme, resulting in the progressive lysosomal accumulation of glucosylceramide (GlcCer) and its deacylated derivate, glucosylsphingosine (GlcSph). GCase is encoded by the GBA1 gene, located on chromosome 1q21 16 kb upstream from a highly homologous pseudogene. To date, more than 400 GBA1 pathogenic variants have been reported, many of them derived from recombination events between the gene and the pseudogene. In the last years, the increased access to new technologies has led to an exponential growth in the number of diagnostic laboratories offering GD testing. However, both biochemical and genetic diagnosis of GD are challenging and to date no specific evidence-based guidelines for the laboratory diagnosis of GD have been published. The objective of the guidelines presented here is to provide evidence-based recommendations for the technical implementation and interpretation of biochemical and genetic testing for the diagnosis of GD to ensure a timely and accurate diagnosis for patients with GD worldwide. The guidelines have been developed by members of the Diagnostic Working group of the International Working Group of Gaucher Disease (IWGGD), a non-profit network established to promote clinical and basic research into GD for the ultimate purpose of improving the lives of patients with this disease. One of the goals of the IWGGD is to support equitable access to diagnosis of GD and to standardize procedures to ensure an accurate diagnosis. Therefore, a guideline development group consisting of biochemists and geneticists working in the field of GD diagnosis was established and a list of topics to be discussed was selected. In these guidelines, twenty recommendations are provided based on information gathered through a systematic review of the literature and two different diagnostic algorithms are presented, considering the geographical differences in the access to diagnostic services. Besides, several gaps in the current diagnostic workflow were identified and actions to fulfill them were taken within the IWGGD. We believe that the implementation of recommendations provided in these guidelines will promote an equitable, timely and accurate diagnosis for patients with GD worldwide.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
BioMed Central  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
BIOMARKERS  
dc.subject
ENZYME ACTIVITY  
dc.subject
GAUCHER DISEASE  
dc.subject
GENETIC TESTING  
dc.subject.classification
Genética Humana  
dc.subject.classification
Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Patient centered guidelines for the laboratory diagnosis of Gaucher disease type 1  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2023-07-11T10:21:14Z  
dc.journal.volume
17  
dc.journal.number
1  
dc.journal.pagination
1-17  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Dardis, A.. Academic Hospital Of Udine; Italia  
dc.description.fil
Fil: Michelakakis, H.. Institute Of Child Health; Grecia  
dc.description.fil
Fil: Rozenfeld, Paula Adriana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Estudios Inmunológicos y Fisiopatológicos. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Estudios Inmunológicos y Fisiopatológicos; Argentina  
dc.description.fil
Fil: Fumic, K.. University Hospital Centre Zagreb; Croacia  
dc.description.fil
Fil: Wagner, J.. No especifíca;  
dc.description.fil
Fil: Pavan, E.. Academic Hospital Of Udine; Italia  
dc.description.fil
Fil: Fuller, M.. University of Adelaide; Australia  
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Fil: Revel Vilk, S.. Shaare Zedek Medical Center; Israel. The Hebrew University of Jerusalem; Israel  
dc.description.fil
Fil: Hughes, D.. University College London; Estados Unidos  
dc.description.fil
Fil: Cox, T.. University of Cambridge; Reino Unido  
dc.description.fil
Fil: Aerts, J.. Leiden Institute of Chemistry; Países Bajos  
dc.journal.title
Orphanet Journal Of Rare Diseases  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://ojrd.biomedcentral.com/articles/10.1186/s13023-022-02573-6  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1186/s13023-022-02573-6