Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep336 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Predictive factors of in-hospital duration of stay in diabetic patients in a medical unit at a university hospital

Mrabet Houcem Elomma , Fadia Boubaker , Elloumi Yesmine , Ayadi Younes , Belkhiri Malak , Wafa Alaya , Baha Zantour , Habib Sfar Mohamed

Background: Patients with diabetes mellitus (DM) have been reported to have longer duration of in-hospital stay (DS). Identifying factors influencing their DS may help in the decision-making process especially in a public health setting.Aim: We aim to compare DS in patients with and without DM admitted to a medical unit in a university hospital and to determine the predictive factors of DS in patients with DM.Methods: A cross secti...

ea0090ep435 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

A case of euglycemic ketoacidosis under iSGLT2 and a review of literature about predictive factors

Fadia Boubaker , Souissi Mariem , Mrabet Houcem Elomma , Ayadi Younes , Baha Zantour , Lassoued Najoua , Wafa Alaya , Habib Sfar Mohamed

Introduction: SGLT2 (sodium-glucose cotransporter 2) inhibitors are a molecule more and more used in type 2 diabetes. However, it can cause a metabolic decompensation in some cases. Euglycemic ketoacidosis may be atypical, misplacing and delaying the diagnosis. We investigated the precipitating factors of this metabolic complication in our case study and in the literature.Presentation of the Case: We report the case of a normal BMI (19 kg/m2) ...

ea0090ep978 | Thyroid | ECE2023

Phenotypic and genetic features of familial thyroid dyshormonogenesis in the Tunisian population

Haj Kacem Akid Faten , Mouhaymen Missaoui Abdel , Soomauroo Siddiqa , Ayadi Younes , Rekik Majdoub Nabila , Mnif Mouna , Abid Mohamed

Objective: To describe the phenotypic and molecular characteristics of familial thyroid dyshormonogenesis (FTDH) in the Tunisian population.Patients and Methods: A retrospective descriptive study including two related (R and K) with high consanguinity whose members are carriers of FTDH. Biological and genetic screening was proposed for all consenting members.Results: FTDH was identified in 11 patients (8 girls, 3 boys) with a mean ...

ea0090p197 | Reproductive and Developmental Endocrinology | ECE2023

Polycystic ovary syndrome phenotype and therapeutic outcomes

Elleuch Mouna , Frikha Hamdi , Ben Salah Dhoha , Triki Molka , Ayadi Younes , Mnif Fatma , Mnif Mouna , Rekik Majdoub Nabila , Charfi Nadia , Haj Kacem Akid Faten , Abid Mohamed

Introduction: Polycystic ovary syndrome (PCOS) is a common endocrinopathy affecting women of reproductive age. PCOS has two phenotypes, obese and lean, the latter being a much less common presentation of the syndrome.Aim: Compare PCOS outcomes in patients with obese PCOS and patients with lean PCOS.Methods: A retrospective, single-center, descriptive and comparative study including patients with PCOS followed at the endocrinology d...

ea0090p519 | Thyroid | ECE2023

Aspects and Evolution of the thyroid gland in Thyroid dyshormonogenesis

Haj Kacem Akid Faten , Mkaouer Samir , Belabed Wafa , Ayadi Younes , Dhieb Nesrine , Mnif Mouna , Rekik Majdoub Nabila , Elleuch Mouna , Abid Mohamed

Introduction: Congenital Hypothyroidism is the principal cause of preventable mental retardation. It is due to Thyroid dysgenesis in 85% of the cases and in 15% to thyroid dyshormonogenesis.Methods: We conducted a prospective study including 17 patients with familial congenital hypothyroidism due to thyroid dyshormonogenesis other than the features of thyroid gland by ultrasound. Other than the phenotype we evaluated the functionality by thyroid Scintigr...

ea0090p797 | Thyroid | ECE2023

Congenital Hypothyroidism and Thyroid dyshormonogenesis: Clinical features and genetic findings

Mkaouer Samir , Haj Kacem Akid Faten , Ayadi Younes , Belabed Wafa , Khochtali Rihab , Noura Bougacha , Rim Chaaben , Ben Salah Dhoha , Abid Mohamed

Introduction: Thyroid dyshormonogenesis represents 15% of congenital hypothyroidism. It is a genetic disorder due to a trouble of Thyroid hormones synthesis. it implies many factors involved in this process mainly TPO Enzyme and NIS channel.Methods: We conducted a prospective study including 17 patients with Congenital Hypothyroidism belonging to 4 consanguine multigenerational Tunisian families. The thyroid dyshormonogenesis was diagnosed based on clini...