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

Internet

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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