Background: In cases of dysostosis, faulty bone development results from embryonic morphogenic abnormalities that take place during the first six weeks of fetal life. Objective: Thisreview aimed tostudy of overview about skeletal dysostosis. Methods: We searched PubMed, Google Scholar, and Science Direct for information on skeletal dysostosis. However, only the most current or comprehensive study from January 1986 to May 2020 was considered. The authors also assessed references from pertinent literature. Documents in languages other than English have been disregarded since there aren't enough resources for translation. Unpublished manuscripts, oral presentations, conference abstracts, and dissertations were examples of papers that weren't considered to be serious scientific research. Conclusion: Modern genetic testing is revolutionizing how uncommon genetic diseases are diagnosed, but appropriate clinical and radiological examination is still necessary. Identifying and preventing potentially serious consequences is important in the management of children with skeletal dysplasia.