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Abstract

October‐December 2017 | Vol. 10 | Issue 4 | Page No 2-3
Camurati-Engelmann Disease: A Case Report
Divya Pachat 1, Krati Shah 1, Wim Van Hul 2, Thambu David 3 and Sumita Danda 1
1Department of Clinical Genetics, Christian Medical College, Vellore, Tamil Nadu, India, 2Department of Medical Genetics, University of Antwerp, Prins Boudewijnlaan 43, 2650 Edegem, Belgium, 3Department of Medicine, Christian Medical College, Vellore, Tamil Nadu, India
Address for Correspondence Email: sdanda@cmcvellore.ac.in
 
Abstract
Among the genetic causes of osteosclerosis, Camurati-Engelmann disease is a rare entity. Bhadada et al. have recently reported the first Indian family with genetic confirmation of Camurati- Engelmann Disease (CED) (Bhadada et al., 2014). Here we describe another case of CED with molecular confirmation.
 
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