ea0056p632 | Clinical case reports - Thyroid/Others | ECE2018
Kanouta Fotini
, Kalaitzidou Styliani
, Triantafillou Eleni
, Drousou Aspasia
, Kyrimis Taxiarchis
, Tampouratzi Dimitra
, Kotis Michalis
, Papadakis Georgios
, Kaltzidou Victoria
, Veniou Eirini
, Drakopoulou Anna
, Karavasili Chrysa
, Mastorakos Georgios
, Tertipi Athanasia
Objectives: Neurofibromatosis type 1 (NF1) is an autosomal, dominant, genetic disorder. The genetic lesion in neurofibromatosis type 1 is located at locus 17q11.2 that harbors the neurofibromin gene. Patients have 3-4 times higher possibility to develop malignancies relative to the general population. The endocrine manifestations of neurofibromatosis include precocious puberty, short stature, osteoporosis and pheochromocytoma. We present a patient with neurofibromatosis type 1...