Searchable abstracts of presentations at key conferences in endocrinology

ea0067o8 | Oral Presentations | EYES2019

Toxic adenoma as a rare cause of hyperthyroidism in a prepubertal boy

Kosteria Ioanna , Vassilakis Ioannis-Anargyros , Koulenti Marina , Voutetakis Antonios , Kanaka-Gantenbein Christina

Background: Toxic adenoma (TA) is a rare cause of hyperthyroidism in children, representing less than 3% of cases, more frequently affecting girls. The risk of malignancy in pediatric autonomous nodules is unknown. Despite current guidelines on the management of TA, published case series reveal discrepancies in medical practice.Case presentation: We report a case of TA in a 7-year old boy, incidentally detected as a palpable mass during examination for l...

ea0067o63 | Oral Presentations | EYES2019

Flash Glucose Monitoring technology in the management of children and adolescents with type 1 Diabetes leads to improved glycemic control

Kosteria Ioanna , Arkoumani Maira , Paschou Stavroula A , Vassilakis Ioannis-Anargyros , Kanaka-Gantenbein Christina

Objective: Flash Glucose Monitoring (FGM) is becoming increasingly popular among children with Type 1 diabetes. Our aim was to evaluate real-life data from children using FGM followed in our center.Methods: We studied 37 patients (51.4% males), with a mean±S.D. age of 10.1±3.9 years at FGM start for a period of 10.1±6.5 months. HbA1c, BMI z-score, number of self-reported and severe hypoglycemias, total insulin daily dose/kg ...

ea0073pep8.4 | Presented ePosters 8: Pituitary and Neuroendocrinology | ECE2021

Whole exome sequencing (WES) reveals oligogenic aetiology in a case of combined pituitary hormone deficiency (CPHD)

Sertedaki Amalia , Tatsi Elizabeth , Vassilakis Ioannis Anargyros , Nikaina Eirini , Fylaktou Eirini , Iacovidou Nikoletta , Siahanidou Soultana , Kanaka-Gantenbein Christina

Background CPHD is characterized by GH and at least one other pituitary hormone deficiency. Mutations in genes expressed in the developing head, hypothalamus, and/or pituitary cause CPHD. To date around 30 genes have been identified to be related to CPHD, however 85% of the cases remain with unknown molecular aetiology.Patient and methodsA newborn boy (46, XY) delivered by CS due to IUGR with a birthweight of...