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<p>* Familial cases where the deletion of chromosome <a href="page.php?w=Chromosome_13_%28human%29">13q14</a> inactivates the <a href="page.php?w=retinoblastoma_gene">retinoblastoma gene</a> is associated with a high risk of osteosarcoma development.<br/>
* Bone dysplasias, including <a href="page.php?w=Paget%27s_disease_of_bone">Paget's disease of bone</a>, <a href="page.php?w=Fibrous_dysplasia_of_bone">fibrous dysplasia</a>, <a href="page.php?w=enchondromatosis">enchondromatosis</a>, and <a href="page.php?w=hereditary_multiple_exostoses">hereditary multiple exostoses</a>,</p><p>
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