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Case Reports
. 2019 Jul 18;12(7):e230660.
doi: 10.1136/bcr-2019-230660.

Hepatomegaly with neutropenia: a girl with glycogen storage disease Ib

Affiliations
Case Reports

Hepatomegaly with neutropenia: a girl with glycogen storage disease Ib

Deepanjan Bhattacharya et al. BMJ Case Rep. .
No abstract available

Keywords: genetics; paediatrics.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Colour photograph showing hair colour before (A) and after corn starch therapy (B).

References

    1. Narisawa K, Otomo H, Igarashi Y, et al. Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase. J Inherit Metab Dis 1982;5:227–8. 10.1007/BF02179148 - DOI - PubMed
    1. Chou JY, Jun HS, Mansfield BC. Neutropenia in type Ib glycogen storage disease. Curr Opin Hematol 2010;17:36–42. 10.1097/MOH.0b013e328331df85 - DOI - PMC - PubMed
    1. Correia CE, Bhattacharya K, Lee PJ, et al. Use of modified cornstarch therapy to extend fasting in glycogen storage disease types Ia and Ib. Am J Clin Nutr 2008;88:1272–6. 10.3945/ajcn.2008.26352 - DOI - PMC - PubMed
    1. Dale DC, Bolyard AA, Marrero TM, et al. Neutropenia In Glycogen Storage Disease 1b (GSD1b). Blood 2013;122:2265.

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