Affiliations: [a] Department of Physical Medicine and Rehabilitation, Harran University Medical School, Sanliurfa, Turkey | [b] Department of Radiology, Harran University Medical School, Sanliurfa, Turkey
Correspondence:
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Corresponding author: Ahmet Boyaci, Assistant professor, MD, Department of Physical Medicine and Rehabilitation, Harran University Medical School, Yenisehir Kampusu 63100, Sanliurfa, Turkey. Tel.: +90 4143182348; Fax: +90 4143181185; E-mail: [email protected]
Abstract: Osteopoikilosis (OPK) is a rare, autosomally inherited, benign sclerosing bone dysplasia of unknown etiology. It is usually found incidentally on radiological examination, presenting as multiple, small, well-defined, variably shaped and widely distributed sclerotic areas throughout the skeleton. In this study, we present a case report of a 56-year-old man suffering from low back pain who was radiologically diagnosed with OPK. His daughter was likewise diagnosed with OPK.
Keywords: Bone dysplasia, familial occurrence, osteopoikilosis, pain
