Successful use of liraglutide in a female patient with type 1 Gaucher disease, type 2 diabetes mellitus and obesity

INTRODUCTION: Gaucher disease is a rare lysosomal storage disease, and caused by a mutation in the GBA1 gene with an autosomal recessive inheritance. Type 1 nonneuronopathic form is the most common form of the disease which commonly presents with painless splenomegaly, anemia, or thrombocytopenia, c...

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Detalles Bibliográficos
Autores principales: Topaloğlu, Ömercan, Ayhan, Ihsan, Tekin, Sakin, Arık, Mina, Bayraktaroğlu, Taner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Obesity, Metabolism and Nutrition
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653160/
http://dx.doi.org/10.1210/jcemcr/luac014.034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10653160/
http://dx.doi.org/10.1210/jcemcr/luac014.034

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