ea0037ep1251 | Clinical Cases–Thyroid/Other | ECE2015
Ayturk Semra
, Genc Ahmet Bilal
, Yaylaci Selcuk
, Gul Serdar Savas
, Tamer Ali
, Celik Mehmet
Osteopoikilosis (OPK) is a rare benign sclerotic bone dysplasia. It is inherited in an autosomal dominant pattern. There is no exact evidence of its aetiology and pathogenesis. Usually, it is an asymptomatic disease and the diagnosis is made incidentally from radiographs which show multiple, small, well-defined, variably shaped and widely distributed sclerotic areas over the skeleton. We report a family with OPK. A 22 years old woman was admitted to outpatient clinic with comp...