hrp0092p1-245 | Multisystem Endocrine Disorders | ESPE2019
Manyas Hayrullah
, Çatli Gönül
, Eroglu Filibeli Berna
, Ayranci Ilkay
, Özdemir Taha Resid
, Dündar Bumin Nuri
Introduction: PTEN Hamartoma Tumor Syndrome (PHTS) is a rare disease with dominant inheritance characterized by benign (hamartoma) and malignant tumors (breast, endometrium, thyroid). Mutations in the tumor suppressor gene phosphatase and tensin homologue (PTEN) gene are responsible for the etiology.Objective: In this case report, we present an 11-year-old male who was being monitored due to follicular thyroid cancer, an...