Endocrine Abstracts

Introduction: Congenital adrenal hyperplasia (CAH) due to 11 beta-hydroxylase deficiency (11βOHD) is a rare autosomal recessive genetic disorder. It results defects in adrenal cortisol and aldosterone synthesis. Early diagnosis and initiation of treatment in male patients are essential in order to prevent serious complications. We report a male patient with CAH who developed complications because of late diagnosisCase Report: 44-year-old male patien...

Introduction: Primary hyperparathyroidism (PHPT) is a disease associated with a decrease in bone mineral density (BMD), especially in cortical bones such as distal radius. Therefore, the BMD measurement of forearm is valuable in the detection of cortical bone loss by PHPT. However, forearm measurement is not routinely recommended for the diagnosis of osteoporosis in PHPT. In this study, we aimed to evaluate the importance and priority of forearm BMD measurement in PHPT.<p ...