Glycogen storage disease (GSD) type III is a metabolic disorder caused by a deficiency in amylo-1,6-glucosidase enzyme, which is responsible for the breakdown of the glycogen molecule, resulting in glycogen accumulating in the organs, hypoglycaemia, muscle weakness, liver dysfunction, delayed anaesthetic recovery, excessive surgical bleeding, cardiomyopathy and end-organ dysfunction. This case report presents a child with GSD type IIIa who underwent orthotopic liver transplantation (OLT) with her mother as a donor. A multidisciplinary approach should be provided to optimise the preoperative period and minimise complications in these patients.
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Hop Antoine Beclere, AP HP, Serv Pediat & Consultat Genet, F-92141 Clamart, FranceHop Antoine Beclere, AP HP, Serv Pediat & Consultat Genet, F-92141 Clamart, France
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Duke Univ, Med Ctr, Div Lab Anim Resources, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Brooks, Elizabeth D.
Yi, Haiqing
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Yi, Haiqing
Austin, Stephanie L.
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Austin, Stephanie L.
Thurberg, Beth L.
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Genzyme, Dept Pathol, Framingham, MA USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Thurberg, Beth L.
Young, Sarah P.
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Young, Sarah P.
Fyfe, John C.
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Michigan State Univ, Lab Comparat Med Genet, E Lansing, MI 48824 USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Fyfe, John C.
Kishnani, Priya S.
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA
Kishnani, Priya S.
Sun, Baodong
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Duke Univ, Med Ctr, Div Med Genet, Durham, NC USADuke Univ, Med Ctr, Div Med Genet, Durham, NC USA