Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1

INTRODUCTION: Gaucher disease (GD) type 1 is a lysosomal disease characterised by hepatosplenomegaly, anemia, thrombocytopenia, bone changes, and bone marrow infiltration. The disease is caused by biallelic pathogenic variants in GBA1 which codes for glucocerebrosidase, an enzyme involved in the cat...

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Detalles Bibliográficos
Autores principales: d'Avila Paskulin, Livia, Starosta, Rodrigo Tzovenos, Zizemer, Vitória Schütt, Basgalupp, Suélen, Bertholdo, Débora, Vairo, Filippo Pinto e, Siebert, Marina, Michelin-Tirelli, Kristiane, Schwartz, Ida Vanessa Doederlein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881662/
https://www.ncbi.nlm.nih.gov/pubmed/31799121
http://dx.doi.org/10.1016/j.ymgmr.2019.100544

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881662/
https://www.ncbi.nlm.nih.gov/pubmed/31799121
http://dx.doi.org/10.1016/j.ymgmr.2019.100544

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