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Articles

Early Radiodiagnosis Of Craniometaphyseal Dysplasia – A Case Report

Authors

  • Kumar Prashant (M.S), Nayana Bhuyan , (M.D) -Medical Officer, Trauma Centre, Banaras Hindu University, Varanasi, U.P, India

Abstract

Craniometaphyseal dysplasia is a rare genetic craniotubular bone remodeling disorder characterized by progressive hyperostosis, undertubulation of the long bones, causing metaphyseal deformities of the long bones, and sclerosis of craniofacial bone. We are reporting a case of craniometaphyseal dysplasia in a 12-year-old indian child, highlighting the importance of radiological diagnosis of this rare genetic disorder.

Article information

Journal

International Journal of Medical Science and Clinical Invention

Volume (Issue)

2 (10)

Pages

Published

2015-10-16

How to Cite

Early Radiodiagnosis Of Craniometaphyseal Dysplasia – A Case Report. (2015). International Journal of Medical Science and Clinical Invention, 2(10). https://valleyinternational.net/index.php/ijmsci/article/view/382

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