Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep234 | Calcium and Bone | ECE2022

Clinical, biological and evolutionary comparison of postsurgical hypoparathyroidism and non-postsurgical hypoparathyroidism

Soomauroo Siddiqa , Mnif Fatma , Mohamed Ahmed Mohamed Abdellahi , Kacem Akid Faten Haj , Charfi Nadia , Mnif Mouna , Abid Mohamed

Introduction: Hypoparathyroidism (HPTH) is an uncommon condition resulting in the production of insufficient amounts of parathyroid hormone (PTH) by the parathyroid glands consequently affecting the calcium phosphate balance. The most frequent etiology of HPTH is the damage to or removal of the parathyroid glands due to a surgery for another condition. Other causes, including autoimmunity and genetic disorders may be responsible for HPTH. Our aim is to compare the different cl...

ea0081ep387 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Screening for distal and symmetric polyneuropathy in the diabetic patient: 116 cases

Elleuch Mouna , Souhir Maalej , Houda Hsine , Ben Salah Dhoha , Mohamed Ahmed Mohamed Abdellahi , Haj Kacem Akid Faten , Abid Mohamed

Introduction: The prevalence of diabetes in the world population is increasing day by day so that its frequency reaches epidemic proportions. As a result, the complications of diabetes are becoming more and more frequent. Diabetic neuropathy, the most common complication which affect up to half of the patients.Purpose of the study: To establish the prevalence of distal symmetrical polyneuropathy (DSPN) in diabetic patients and demonstrate the importance ...

ea0081ep620 | Endocrine-Related Cancer | ECE2022

A NEM 2A with mutation in a gene outside panel ROTERC

Abdellahi Mohamed Ahmed Mohamed , Mejdoub Nabila , Souhir Guidara , Salah Dhoha Ben , Mnif Mouna , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Multiple endocrine neoplasia type 2 is an inherited syndrome characterized by the characteristic combination of medullary thyroid cancer, pheochromocytoma and primary hyperparathyroidism. We report one case with phenotype-genotype mismatch.Observation: Patient A. T is 45 years of age with a family history of thyroid bone marrow cancer (CMT) and sister brain cancer, father colon cancer, with no personal history of disease. A 60 mm long-axis ...

ea0081p346 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Combination study of apoptosis gene polymorphisms in mitochondrial diabetes: Potential role in the pathogenesis of mitochondrial diabetes

Kacem Akid Faten Haj , Mohamed Ahmed Mohamed Abdellahi , Nesrine Dhieb , S Youssef , E Mkaouar-Rebai , F Fakhfakh , Mnif Mouna , Abid Mohamed

Introduction: Mitochondrial diabetes (DM) is a monogenic form of maternal transmission diabetes that is caused by mutations in the mitochondrial genome. These mutations affecting mitochondrial function may be the cause of initiation of the phenomenon of apoptosis itself having an aggravating role of the phenotype in patients with mitochondrial diabetes.Materials and Methods: This study involved 43 patients with mitochondrial diabetes (20 non-syndromic an...

ea0081ep312 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Clinical characteristics and glycemic control in Tunisian patients with type 2 diabetes suffering from lower urinary tract dysfunctions: a comparative population-based survey

Haj Kacem Akid Faten , Missaoui Abdelmouhaymen , Behoul Mariem , Mohamed Ahmed Mohamed Abdellahi , Belabed Wafa , Ben Salah Dhoha , Fatma Mnif , Rekik Majdoub Nabila , Elleuch Mouna , Abid Mohamed

Background and Aims: Several studies have pointed a significant relationship between diabetic complications, glycemic imbalance, and the onset of lower urinary tract dysfunction (LUTD) in this population. The current survey aims to assess the clinical and biochemical characteristics related to glycemic control in patients with type 2 diabetes presenting with symptoms of LUTD.Patients and Method: We conducted a comparative cross-sectional study that inclu...

ea0081ep531 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Type 1 diabetes, metabolic syndrome and cardiovascular risk

Mohamed Ahmed Mohamed Abdellahi , Salah Dhoha Ben , Soomauroo Siddiqa , Elleuch Mouna , Mnif Mouna , Mejdoub Nabila , Akid Faten Haj Kacem , Abid Mohamed

Introduction: Metabolic syndrome (MS) is responsible for the increased cardiovascular risk in type 2 diabetics, but few studies have looked at the metabolic syndrome in type 1 diabetics. The aim of This study is to evaluate the prevalence of microvascular and macrovascular complications and evaluate the cardiovascular risk among patients with T1DM associated with metabolic syndrome.Materials and Methods: Retrospective study which included 36 type 1 diabe...

ea0081ep970 | Thyroid | ECE2022

Autoimmune thyroid disorders and connective tissue disease

Salah Raida Ben , Akid Faten Haj Kacem , Soomauroo Siddiqa , Mohamed Ahmed Mohamed Abdellahi , Chouaib Sarra , Frikha Faten , Rekik Nabila , Abid Mohamed , Bahloul Zouheir

Introduction: Mixed connective tissue disease (MCTD), also known as Sharp´s syndrome is a rare autoimmune disease (AD), characterized by the presence of high titers of a distinctive autoantibody: ribonucleoprotein auto-antibody (anti-RNP). It presents with varied overlapping symptoms of different connective tissue disorders which may appear sequentially over time. As other AD, MCTD may be associated with one or more AD, such as autoimmune thyroid disorders (AITD).<p c...

ea0081p712 | Reproductive and Developmental Endocrinology | ECE2022

Phenotypic and genotypic heterogeneity of sexual development disorders 46, XY in the Tunisian population

Haj Kacem Akid Faten , Abdellahi Mohamed Ahmed Mohamed , Nessrine Dhieb , B Benrhouma , T Kammoun , M Hachicha , N Kallel , N Belguith , Mnif Mouna , Abid Mohamed

Introduction: Sexual disorders 46 XY DSD are responsible for a range of phenotypic disorders, ranging from an ambiguous phenotype to a complete female phenotype. In this context, we report a cohort of 22 46 XY patients with a female phenotype in order to establish a phenotype-genotype correlation.Results: The average age at diagnosis was 15.5 years (E: 7 days-33 years). The reason for consultation was primary amenorrhea in 16 cases (72.7%), sexual ambigu...

ea0073ep199 | Thyroid | ECE2021

Unmasked Graves’ disease following tamoxifen withdrawal

El ArbI Kawthar , Safi Wajdi , Boujelben Khouloud , Mohamed Abdellahi Mohamed Ahmed , Mohamed Elmoctar Sidina , Mejdoub Nabila , Mnif Mouna , Kacem Faten Hadj , Mohamed Abid

IntroductionThe synthetic anti-oestrogen tamoxifen is the endocrine treatment modality most commonly used for therapy of hormone sensitive breastcancer. The influence of tamoxifen on thyroid function has not been fully elucidated.ObservationA 46-year-old female patient who presented a GravesÂ’ disease diagnosed 10 years ago. She had a moderate vascular goiter and no ocular signs. She presented firstly a s...