1. PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose
- Author
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Voermans, N.C., Preisler, N., Madsen, K.L., Janssen, M.C.H., Kusters, B., AbuBakar, N. Bin, Conte, F., Lamberti, V.M., Nusman, F., Engelen, B.G.M. van, Scherpenzeel, M. van, Vissing, J., Lefeber, D.J., Voermans, N.C., Preisler, N., Madsen, K.L., Janssen, M.C.H., Kusters, B., AbuBakar, N. Bin, Conte, F., Lamberti, V.M., Nusman, F., Engelen, B.G.M. van, Scherpenzeel, M. van, Vissing, J., and Lefeber, D.J.
- Abstract
Contains fulltext : 169774.pdf (publisher's version ) (Closed access), Mutations in PGM1 (phosphoglucomutase 1) cause Glycogen Storage Disease type XIV, which is also a congenital disorder of protein N-glycosylation. It presents throughout life as myopathy with additional systemic symptoms. We report the effect of oral galactose treatment during five months in a patient with biochemically and genetically confirmed PGM1 deficiency. The 12-minute-walking distance increased by 225 m (65%) and transferrin glycosylation was restored to near-normal levels. The exercise assessments showed a severe exercise intolerance due to a block in skeletal muscle glycogenolytic capacity and that galactose treatment tended to normalize skeletal muscle substrate use from fat to carbohydrates during exercise.
- Published
- 2017