Searchable abstracts of presentations at key conferences in endocrinology

ea0035p264 | Clinical case reports Thyroid/Others | ECE2014

Primary hyperparathyroidism with severe hypercalcemia during pregnancy

Akin Fulya , Erturk Mehmet Sercan , Yaylali Guzin Fidan , Soysal Ergun

Introduction: Primary hyperparathyroidism (PHPT) commonly goes unrecognized due to the physiological changes of pregnancy.PHPT is associated with significant maternal and fetal morbidity and mortality. Current evidence supports parathyroidectomy is the main treatment, performed preferably during the second trimester, when the serum calcium is above 11–mg/dl. We report the clinical course of a woman with newly diagnosed gestational PHPT who refused minimally invasive parat...

ea0037ep1261 | Clinical Cases–Thyroid/Other | ECE2015

Atypical subacute thyroiditis

Yaylali Guzin Fidan , Ok Zeynep Dundar , Erturk Mehmet Sercan , Akin Fulya , Topsakal Senay

Introduction: A diagnosis of subacute thyroiditis (SAT) is readily suspected when patients present with a particular set of typical clinical and laboratory characteristics. We present a patient with atypical SAT who had no neck pain but presented with fever, and weight loss; had thyrotoxicosis with normal 99mTc uptake, and needed higher doses of steroids to resolve.Case report: A 57-year-old man presented with a fever (39  °C) of 2 month-durati...

ea0035p263 | Clinical case reports Thyroid/Others | ECE2014

Coexisting hurthle cell neoplasm and thyroid hormone resistance

Yaylali Guzin Fidan , Erturk Mehmet Sercan , Akin Fulya , Yalcin Nagihan , Gurkan Hakan , Ozden Akin , Guldiken Sibel

Introduction: Resistance to thyroid hormone (RTH) is an inherited syndrome characterized by reduced responsiveness of target tissues to thyroid hormone (TH). It is characterized by high serum concentrations of free T4 (Ft4) and usually free T3 (Ft3) accompanied by normal or slightly high serum TSH concentrations. When RTH is suspected, the diagnosis should be confirmed by direct sequencing of the TR-β gene to identify mutations....

ea0035oc9.5 | Reproduction | ECE2014

IGF1 gene polymorphism in Polycystic Ovary Syndrome

Tural Mehmet , Akin Fulya , Turgut Sabahat , Yaylali Guzin Fidan , Ata Melek Tunc , Ozkan Seyma , Erturk Mehmet Sercan

Introduction: IGFs (Insulin like growth factors) are important regulators of pancreatic β-cell development, growth and maintanence. Mutations in the IGF genes have been found to be associated with type 2 diabetes, myocardial infarction, birth weight and obesity. These associations could result from changes in insulin secretion. Insulin resistance plays a key role in PCOS. Based on these findings, we aimed to investigate IGF1 gene polymorphism in polycystic ovary syndrome ...