ea0026p438 | Thyroid (non cancer) | ECE2011
Altay Mustafa
, Colbay Mehmet
, Toruner Fusun Balos
, Akturk Mujde
, Sancar Erkam
, Cakir Nuri
, Arslan Metin
Introduction: Werner syndrome (WS) is an autosomal recessive disease characterized by premature aging, skin changes, gray hair, alopecia, muscle atrophy, osteoporosis, and cataracts and has a high frequency of association with rare neoplasms. In addition, some endocrinological abnormalities were manifested in this rare disease, such as hypogonadism, diabetes mellitus, hyperlipidemia. Atrophic changes of organs and systems such as skin, brain and genital organs were reported. H...