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Endocrine Abstracts (2023) 90 EP567 | DOI: 10.1530/endoabs.90.EP567

National Institute of Nutrition of Tunis, C, Tunis, Tunisia


Introduction: Monogenic diabetes MODY is common but remains under diagnosed because genetic study is expensive in our country.

Method: We report the case of an 18-year-old patient with no personal pathological history admitted in October 2022 for diabetes management. Her diabetes was diagnosed accidentally on July 2022: Systematic capillary blood glucose done when she had a Hysteria’s crisis revealed values higher than 2 g/l. From July to October, the patient did not received any antidiabetic treatment and never had any acute complication, especially ketoacidosis one. Our patient did not have cardinal signs of diabetes. The physical examination showed acanthosis nigricans and overweight (BMI=25.7 kg/m2). HbA1c was 9.9%, insulinemia and C-peptide were normal, and HOMA index was 2.52. Thyroid parameters and basal cortisolemia were normal. There were no pancreatic autoimmunity (negative anti-GAD 65, anti-islets and anti-insulin antibodies). The “MODY RISK” score was at 75%. The association of polycystic ovary syndrome or polycystic kidney disease was ruled out by radiological examinations. The patient was put on Glimepiride 1 mg/d and Metrormine 850 1 cp/d with achievement of glycemic targets. The genetic study was requested in progress.

Conclusion: Monogenic diabetes MODY has common characteristics with T1D and T2D. It is often underdiagnosed due to the cost of genetic study but it should be evoked when diabetes presentation is atypical.

Volume 90

25th European Congress of Endocrinology

Istanbul, Turkey
13 May 2023 - 16 May 2023

European Society of Endocrinology 

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