PEN-HUA SU2026-10-162026-10-162011-02-01Pure ID: 15426400Pure UUID: 89b6837e-5aea-4710-b0be-e8ecf45b6cdd10.1016/j.pedneo.2010.12.001https://www.scopus.com/pages/publications/79952455585https://scholars.csmu.edu.tw/handle/123456789/33681Structural anomalies associated with partial 2p monosomy are rare. There has only been one case of interstitial deletion of 2p24.2-2p25.1 and three cases of 2p23.3-2p25.1 described in the literature. We report here the first instance of an interstitial deletion of 2p23p24, confirmed by comparative genome hybridization. We present a clinical and cytogenetic report of a patient with psychomotor retardation, hearing impairment, and limb abnormalities. The obvious osseous fusion with bone marrow and cortex continuation between proximal parts of radius and ulna - congenital radioulnar synostosis - were first visualized by multidetector-row computed tomography scan.5enjournal article