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A patient with glycogen storage disease type Ib presenting with acute myeloid leukemia (AML) bearing monosomy 7 and translocation t(3;8)(q26;q24) after 14 years of treatment with granulocyte colony-stimulating factor (G-CSF): A case report

INTRODUCTION: Glycogen storage disease type Ib is an autosomal recessive transmitted disorder of glycogen metabolism caused by mutations in the glucose-6-phosphate translocase gene on chromosome 11q23 and leads to disturbed glycogenolysis as well as gluconeogenesis. Besides hepatomegaly, growth reta...

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Detalles Bibliográficos
Autores principales:	Schroeder, Thomas, Hildebrandt, Barbara, Mayatepek, Ertan, Germing, Ulrich, Haas, Rainer
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2008
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2566578/ https://www.ncbi.nlm.nih.gov/pubmed/18826620 http://dx.doi.org/10.1186/1752-1947-2-319

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