ea0037ep1293 | Clinical Cases–Thyroid/Other | ECE2015
Tuzun Dilek
, Oguz Ayten
, Sahin Murat
, Kaleli Ilhami Taner
, Bakaris Sevgi
, Deniz Mustafa Saygin
, Cabioglu Cansu Yilmaz
, Gul Kamile
Introduction: Multiple endocrine neoplasia type 2A (MEN2A) is a complex autosomal dominant inherited syndrome characterized by medullary thyroid carcinoma (MTC), phaeochromocytoma, and primary parathyroid hyperplasia (PPH). In patients with only one or two clinical features, identification of a germline rearranged in transfection (RET) mutation or the identification of the clinical features of MEN2A in other first degree relatives is required to make the diagnosis. We present ...