Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep262 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Diabetic health literacy and its association with medication adherence among adult patients with type 2 diabetes mellitus

Marrakchi Meriem , Tira Sarra , Gargoury Mouna

Introduction: Poor adherence to prescribed diabetic medication is a major contributor to disparities in effective glycemic control among patients with type 2 diabetes mellitus. The purpose of this study was to investigate the association between health literacy level and adherence to diabetic medications among this population.Methods: A cross-sectional survey enrolled 66 patients medically treated for type 2 diabetes mellitus. Patients with dementia synd...

ea0056p394 | Diabetes (to include epidemiology, pathophysiology) | ECE2018

Mitochondrial diabetes in 40 patients belonging to 30 Tunisian families: phenotypic and genotypic heterogeneity

Safi Wajdi , Tabbabi Mouna , Hadj Kacem Faten , Gargouri Imene , Elleuch Mouna , Sassi Salwa , Mnif Feki Mouna , Fakhfakh Faiza , Abid Mohamed

Introduction: Mitochondrial diabetes (MD) is characterized by a broad spectrum of phenotypic and genotypic involvement. Through a cohort study of 40 patients with DM, we tried to correlate this diversity of phenotypic expression with the biomolecular substratum of the mitochondrial genome in the Tunisian population.Results: Epidemiologically and anthropometrically, our series fits the literature data with age at 31.6 years (5–52), female predominanc...

ea0063p834 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

Familial multiple endocrine neoplasia type 1 revealed by a maxillary swelling

Salah Dhouha Ben , Gargouri Imen , Mnif Fatma , Elleuch Mouna , Charfi Nadia , Mnif Mouna , Rekik Nabila , Abid Mohamed

Introduction: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder caused by mutations in the MEN1 tumor suppressor gene and is characterized clinically by tumors in two or more endocrine glands, such as the pituitary gland, parathyroid glands or pancreatic islets. We describe an atypical presentation of familial hyperparathyroidism evoking the diagnosis of MEN1 in the first place.Observations: We report a three-member family....

ea0056p1109 | Thyroid (non-cancer) | ECE2018

Congenital hypothyroidism: genes involved in organogenesis disorders

Chaabane Rim , Gargouri Imen , Hadjkacem Faten , Mrabet Houssem , Elleuch Mouna , ghorbel Dorra , Mnif Mouna , Charfi Nadia , Belguith Neila , Abid Mohamed

Introduction: Congenital hypothyroidism (CH) is the most common congenital endocrine disease since it affects 1/3000–1/4000 births. The involvement of genetics is no longer discussed and several genes have been implied in the different clinical forms of thyroid dysgenesis.Patients and methods: We report ten cases of thyroid dysgenesis collected at the pediatric and endocrinology departments of Sfax in Tunisia. The diagnosis was based on clinical, bi...

ea0063p987 | Diabetes, Obesity and Metabolism 3 | ECE2019

Epidemiological, clinical and biochemical characteristics of metabolic syndrome in adults living in South of Tunisia

Chabchoub Ghazi , Gargouri Imene , Kacem Faten Hadj , Charfi Nadia , Mnif Mouna , Keskes Leila , Abid Mohamed

The metabolic syndrome (MetS) is a constellation of physiological and biochemical abnormalities characterized by obesity, hyperglycaemia, elevated triglycerides and decreases in high density lipoprotein cholesterol (HDL-C), and hypertension. The MetS promotes atherosclerosis, and increases the risk of developing diabetes and cardiovascular disease (CVD), as well as rates of mortality. Thus, it has become one of the major public health challenges worldwide. In Tunisia, few stud...

ea0063p1058 | Pituitary and Neuroendocrinology 3 | ECE2019

Pituitary apoplexy: diagnosis, management and outcome in 44 patients

Gargouri Imen , Hadjkacem Faten , Mnif Mouna , Walha Mohamed , Rekik Nabila , Charfi Nadia , Ayadi Fatma , Abid Mohamed

Introduction: Pituitary apoplexy (PA) is a rare incident defined by the occurrence of necrosis and/or haemorrhage of the pituitary gland. PA is a clinical syndrome characterized by the sudden onset of headache, vomiting, visual impairment and decreased consciousness in some cases. The objectives of our study are to describe its clinical, biological and imaging features as well as the management of PA in the region of Sfax.Patients and methods: It is a re...

ea0063p1213 | Thyroid 3 | ECE2019

Hyperthyroidism and hepatic dysfunction: the impact of congestive heart failure

Benothman Wafa , Kacem Faten Hadj , Gargouri Imen , Elleuch Mouna , Mnif Fatma , Abid Mohamed

Introduction: Hyperthyroidism (HT) has been associated with hepatic dysfunction in the presence or absence of congestive heart failure (CHF). Our objective is to study the correlation between the clinical and biological presentation of hepatic abnormalities and the cardiac status.Patients and methods: This retrospective study included 17 patients hospitalized in the endocrinology department of Hedi Chaker Hospital in Sfax over 20 years (1997–2017). ...

ea0070aep688 | Pituitary and Neuroendocrinology | ECE2020

Do cardiovascular risk factors predispose to pituitary apoplexy?

Gargouri Imen , Faten Hadjkacem , Othman Wafa Ben , Mouna Mnif , Mohamed Abid

Introduction: Pituitary apoplexy (PA) is a rare incident defined by the occurrence of necrosis and/or haemorrhage of the pituitary gland. The low incidence of PA makes it difficult to bring out from the studies its precipitating factors and especially its relationship with cardiovascular risk factors (CVR). The objectives of this studies were to characterize a number of patients with PA and to establish the link between PA and their CVRs.Methods: It is a...

ea0056p144 | Female Reproduction | ECE2018

Female fertility in congenital adrenal hyperplasia

Gargouri Imen , Mnif Fatma , Ajili Rihab , Hadjkacem Faten , Sessi Salwa , Kammoun Mahdi , Mnif Mouna , Abid Mohamed

Introduction: Congenital adrenal hyperplasia (CAH) is a genetic disease with autosomal recessive inheritance. The deficit in 21-hydroxylase (21-OH) is by far the most common enzyme deficiency CAH, since it represents 95% of the cases. Fertility in wome is found to be reduced due to hormonal, mechanical and psychological factors.Patients and methods: It is about a descriptive and prospective study conducted in 15 patients collected in the endocrinology de...

ea0099ep1076 | Diabetes, Obesity, Metabolism and Nutrition | ECE2024

Accuracy of urine dipstick tests for assessment of glucosuria

Gargouri Omar , Marrakchi Rim , Mezghani Ines , Mariem Boudaya , Jammoussi Kamel , Turki Mouna

Introduction: Early diagnosis is therefore important for patients with asymptomatic diabetes mellitus. The aim of this study is to validate the use of Urine Dipstick in the screening of glycosuria (Gu).Material and methods: Our study involved 30 fresh urine specimens. Urinalysis was performed by dipstick (SPINREAT®). Gu was measured by the hexokinase method (DxC800® Beckman Coulter). The gold standard to diagnose Gu was co...