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. 2025 Jun 5.
doi: 10.1007/s00592-025-02524-0. Online ahead of print.

Advanced hybrid closed loop system (MiniMed 780G) achieving significant improvement of glucose control in a patient with maternally inherited diabetes and deafness: a case report

Michalis K Picolos  1   2 , Anastasia Papapostolou  3   4 , Anastasia Christodoulou  5 , George A Tanteles  6   7 , Anna Kyriakidou  8 , Georgios Papaetis  9   10
Affiliations

Advanced hybrid closed loop system (MiniMed 780G) achieving significant improvement of glucose control in a patient with maternally inherited diabetes and deafness: a case report

Michalis K Picolos et al. Acta Diabetol. .
No abstract available

Keywords: AHCL; AID; Advanced hybrid closed loop; Insulin pump; MIDD; Maternally inherited diabetes and deafness; Medtronic.; MiniMed 780G; Mitochondrial diabetes.

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Conflict of interest statement

Declarations. Conflict of interest: The authors declared thaat they have no conflict of interest. Informed patient consent for publication: Signed informed consent was, g6g obtained directly from patient.

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References

    1. Yang M, Xu L, Xu C, Cui Y, Jiang S, Dong J et al (2021) The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients. Front Endocrinol 12:728043 - DOI
    1. Kyriakidou A, Hadjivassiliou M, Papapostolou A, Picolos MK (2023) Maternally inherited diabetes and deafness (MIDD)—atypical clinical diabetes features leading to the diagnosis. JCEM Case Rep 1(3):luad047 - DOI - PubMed - PMC
    1. Murphy R, Turnbull DM, Walker M, Hattersley AT (2008) Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A > G mitochondrial point mutation. Diabet Med 25(4):383–399 - DOI - PubMed
    1. Parikh S, Goldstein A, Koenig MK, Scaglia F, Enns GM, Saneto R et al (2015) Diagnosis and management of mitochondrial disease: a consensus statement from the mitochondrial medicine society. Genet Med 17(9):689–701 - DOI - PubMed
    1. Salles JE, Moisés VA, Almeida DR, Chacra AR, Moisés RS (2006) Myocardial dysfunction in mitochondrial diabetes treated with coenzyme Q10. Diabetes Res Clin Pract 72(1):100–103 - DOI - PubMed

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