hrp0086p2-p721 | Endocrinology and Multisystemic Diseases P2 | ESPE2016
Ucar Ahmet
, Yetim Aylin
, Battal Muharrem
, Pinarli Ferda Alparslan
, Kilic Evrim
, Tuncel Deniz
, Ozturk Feyza Yener
, Kaya Reyhan
, Oral Arzu
, Genc Ozgur
Background: Multiple endocrine neoplasia (MEN)1 is a rare autosomal dominant disorder with primary hyperparathyroidism, enteropancreatic neuroendocrine tumors and anterior pituitary adenomas.Patient: A16-yr-old male was referred to our center due to recurrent seizures. Family history was significant for maternal death due to metastatic adenocarcinoma of the lung,paternal history of low-grade liposarcomas and nephrolitiasis. Physical examination was norma...