Searchable abstracts of presentations at key conferences in endocrinology
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European Congress of Endocrinology 2021

Online
22 May 2021 - 26 May 2021

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The European Congress of Endocrinology provides a global platform for the international endocrine community to discuss the latest advances in the field.

Eposter Presentations

General Endocrinology

ea0073ep132 | General Endocrinology | ECE2021

The prevalence of common risk factors for depression development in diabetes mellitus of the type 2

Navmenova Yana , Makhlina Elena

ObjectiveTo evaluate the frequency of common risk factors for depression development in patients with the diabetes mellitus of the type 2 (DM 2).Materials and methods163 patients with DM 2 at the age of 40–65 years old, period of DM is 11.18 [4.28; 22.33] years. The evaluation of the anxiety and depression level was carried out with the use of the Hospital anxiety and depression scale (HADS); a ...

ea0073ep133 | General Endocrinology | ECE2021

Severe hypertriglyceridemia in young adults

Gherissi Wiem , Kacem Faten Hadj , Ben Salah Dhoha , Zargni Asma , Mahjoub Rkik Nabila , Mnif Mona , Mnif Fatma , Charfi Nedia , Elleuch Mona , Abid Mohamed

IntroductionSevere hypertriglyceridemia (sHTG) (plasma triglycerides b 10 g/l) is a rare but pernicious and understudied condition.ObjectiveOur objective was to evaluate the etiology, characteristics, and complications of sHTG.MethodsIt’s a retrospective study including 10 patients with (sHTG) diagnosed between 1998 and 2020, at the department of endocri...

ea0073ep134 | General Endocrinology | ECE2021

Autoimmune polyglandular syndrome type 3: a case report

Besrour Chayma , Rojbi Imen , Laamouri Rihab , Lakhoua Youssef , Mchirgui Nadia , Ben Nacef Ibtissem , Khiari Karima

IntroductionAutoimmune polyglandular syndrome (APS) is a rare endocrinopathy, characterized by the coexistence of two or more glandular autoimmune diseases that can appear at different intervals of time.ObservationHerein the case of a young woman descendant of first degree consanguineous marriage, diagnosed since the age of six with celiac disease (CD) where gluten-free diet was not respected due to poor soci...

ea0073ep135 | General Endocrinology | ECE2021

Multiple endocrine neoplasia type 1 presenting with foreneck swelling

Fen-Yu Tseng , Wan-Chen Wu

IntroductionMultiple endocrine neoplasia type 1 (MEN-1) is a hereditary condition with neoplastic lesions in multiple endocrine organs, which most frequently involves pituitary, parathyroid gland, and pancreas.Case reportA 53 y/o male visited endocrine clinic with the chief complaint of foreneck swelling for 1 month. He had history of renal stone for years. He had normal fT4 (1.13 ng/dl, reference 0.93–1...

ea0073ep136 | General Endocrinology | ECE2021

Clinical implications for the variations in the BMI in the clinical trial population with obstructive sleep apnea and narcolepsy evaluated for excessive sleepiness with Solriamfetol: a rapid review

Trivedi Shailesh , Trivedi Akta

IntroductionSolriamfetol is a dopamine and norepinephrine reuptake inhibitor, indicated to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA). Decrease in the body weight as an adverse effect of < 2% incidence in both the narcolepsy and OSA patients has been reported. We hypothesise that the baseline Body Mass Index (BMI) may be a an independent predictive marker for the...

ea0073ep137 | General Endocrinology | ECE2021

Extra-digestive manifestations of celiac disease

Akkari Imen , Raida Harbi , Soumaya Mrabet , Jazia Elhem Ben

IntroductionCeliac disease is an autoimmune enteropathy secondary to gluten intolerance developing in genetically predisposed patients. The atypical presentation is the most common form of the disease. The aim of this work is to report the various extradigestive manifestations associated with celiac disease.Patients and methodsThis is a descriptive transversal study carried out over a period of 10 years. All ...

ea0073ep138 | General Endocrinology | ECE2021

Functional hypoglycemia: clinical and biological characteristics

Kamoun Elyes , Mekni Sabrine , Rojbi Imen , Mchirgui Nadia , Lakhoua Youssef , Ben Nacef Ibtissem , Khiari Karima

IntroductionAs hypoglycemia is a common symptom, an organic cause is always the first diagnosis looked for as it can be associated with a specific medical or surgical treatment. Diagnosis of functional etiology isn’t as precise, as the whipple triad can be incomplete. We herein report a serie of confirmed etiology for functional hypoglycemia.MethodsThis is a descriptive retrospective study including 20 c...

ea0073ep139 | General Endocrinology | ECE2021

Vitamin D status and the association with metabolic risk factors in polycystic ovarian syndrome patients attending a tertiary hospital of Morocco

Ben Yakhlef Salma , Bouichrat Nisrine , Abdellaoui Wahiba , Rouf Siham , Latrech Hanane

IntroductionPolycystic ovary syndrome (PCOS) is the most common female endocrine disorder with a prevalence of 8– 13% in women of reproductive age. Accumulating evidence suggests that vitamin D deficiency might have multiple impacts on the disease process ; and is involved in the pathogenesis of metabolic syndrom in PCOS. This notion is carried by the fact that the vitamin D receptor gene regulates about 3% of the human genome. The purpose of this s...

ea0073ep140 | General Endocrinology | ECE2021

Thrombosis and coeliac disease

Akkari Imen , Raida Harbi , Soumaya Mrabet , Jazia Elhem Ben

IntroductionThe occurrence of thromboembolic events in celiac disease has been reported in the literature, especially in adults. The objective of our study is to determine the prevalence and clinical characteristics of thrombosis in celiac disease and to clarify the role of thrombophilic factors.Patients and methodsThis is a retrospective series of four observations of thrombosis among a cohort of 41 patients...

ea0073ep141 | General Endocrinology | ECE2021

Wermer syndrome: different phenotypes for the same disorder

Halloul Imen , Ben Abdelkerim Asma , Khaldi Safa , Saad Ghada , Kacem Maha , Chaieb Molka , Maaroufi Amel , Hasni Yosra , Ach Koussay

IntroductionWerner syndrome (WS) is a rare genetic disorder that displays clinical features suggestive of accelerated aging. Also known as adult progeria, it is caused by mutations in the WRN gene, which encodes a RecQ DNA helicase. Primary characteristics of this syndrome are progeroid changes of hair, bilateral cataract, atrophic skin, soft-tissue calcification, bird-like face, abnormal voice and many others features. Here we report 5 patients...

ea0073ep142 | General Endocrinology | ECE2021

K+-dependent Na+/Ca2+ -exchangers 3 aggravates experimental colitis in mice

Eui-Bae Jeung , Nam Tran Dinh , Yi Donglin , Min Kim Kang

Calcium signaling plays a regulatory role in the events of cellular proliferation. In immunocytes such as T cells, B cells, mast cells and many other cell types, Ca2+ signals show to control the proliferation, differentiation, and function. Furthermore, Ca2+ has been shown to act as a second messenger to regulate innate immune cell function and activation. Here, we found that loss of Nckx3, a potassium-dependent Na+ /Ca2+</...