Case reportA 16-year-old girl presented to our clinic with growth retardation. She was born after 40 weeks gestation by vaginal delivery with a birth weight of 3,100 g. Her past medical and surgical histories were unremarkable. She had no familial history of thyroid or autoimmune disease. Her history revealed that she had been previously healthy but had experienced a diminished growth rate since the age of six. On physical examination, her height was 142.6 cm ( 3 ˂ rd percentile), and her weight was 43.6 kg ( 10 ˂ th percentile). Her thyroid gland was not palpable. Her breasts were enlarged bilaterally (Tanner stage IV) and pubic hairs were present (Tanner stage IV). She was amenorrhea. The neurological examination including full visual fields was normal. Laboratory data revealed hypercholesterolemia (350 mg/ dL), and hypertriglyceridemia (476 mg/dL). Endocrinological investigations revealed decreased thyroid function (free thyroxine [T4], 2.31 pmol/L; TSH ˃ 100 mIU/L), elevated serum prolactin level (74.2 ng/mL) and normal sex hormones (follicle stimulating hormone [FSH], 5.