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Case Reports
. 2013 Sep;36(9):e135-6.
doi: 10.2337/dc13-0724.

Difficult management of glucose homeostasis in a 21-month-old child with type 1 diabetes and unknown glutaric aciduria type I: a case report

Marco Marigliano, Genan Anton, Alberto Sabbion, Anita Morandi, Grazia Morandi, Daniela Degani, Claudio Maffeis
Case Reports

Difficult management of glucose homeostasis in a 21-month-old child with type 1 diabetes and unknown glutaric aciduria type I: a case report

Marco Marigliano et al. Diabetes Care. 2013 Sep.
No abstract available

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Figures

Figure 1
Figure 1
Brain magnetic resonance imaging. The arrows show the hyperintense signal of the caudate nuclei and putamina, as typically happens in patients with GA-I.
See this image and copyright information in PMC

References

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    1. Goodman SI, Stein DE, Schlesinger S, et al. Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations. Hum Mutat 1998;12:141–144 - PubMed
    1. Zschocke J, Quak E, Guldberg P, Hoffmann GF. Mutation analysis in glutaric aciduria type I. J Med Genet 2000;37:177–181 - PMC - PubMed
    1. Kölker S, Garbade SF, Greenberg CR, et al. Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res 2006;59:840–847 - PubMed

MeSH terms

Supplementary concepts