مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Cites:

1

Information Journal Paper

Title

GCK MUTATION IN A CHILD WITH MATURITY ONSET DIABETES OF THE YOUNG, TYPE 2

Pages

  226-228

Abstract

 Background: Maturity onset DIABETES of the young type 2 (MODY) is an inherited disorder due to mutations in glucokinase (GCK) gene, which lead to mild FASTING HYPERGLYCEMIA.Case Presentation: Herein an otherwise healthy 9-year old boy with hyperglycemia is presented in whom the diagnosis of MODY2 was suspected. Genetic studies showed heterozygous inactivating GCK gene mutation in exon 8 (c.1010delA) in this patient. The same mutation was found in his father as well. The patient received some dietary advices without any medication.Conclusion: The identification of GCK mutation and diagnosis of MODY2 helps the clinicians to predict the disease course, prognosis and to exclude other types of DIABETES.

Cites

References

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  • Cite

    APA: Copy

    NOORIAN, SHAHAB, SAYARIFARD, FATEMEH, FARHADI, ELHAM, BARBETTI, FABRIZIO, & REZAEI, NIMA. (2013). GCK MUTATION IN A CHILD WITH MATURITY ONSET DIABETES OF THE YOUNG, TYPE 2. IRANIAN JOURNAL OF PEDIATRICS, 23(2), 226-228. SID. https://sid.ir/paper/652362/en

    Vancouver: Copy

    NOORIAN SHAHAB, SAYARIFARD FATEMEH, FARHADI ELHAM, BARBETTI FABRIZIO, REZAEI NIMA. GCK MUTATION IN A CHILD WITH MATURITY ONSET DIABETES OF THE YOUNG, TYPE 2. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2013;23(2):226-228. Available from: https://sid.ir/paper/652362/en

    IEEE: Copy

    SHAHAB NOORIAN, FATEMEH SAYARIFARD, ELHAM FARHADI, FABRIZIO BARBETTI, and NIMA REZAEI, “GCK MUTATION IN A CHILD WITH MATURITY ONSET DIABETES OF THE YOUNG, TYPE 2,” IRANIAN JOURNAL OF PEDIATRICS, vol. 23, no. 2, pp. 226–228, 2013, [Online]. Available: https://sid.ir/paper/652362/en

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