| Literature DB >> 12420919 |
J P Soni1, B D Gupta, M Soni, V Mund, Rajesh Aneja.
Abstract
Engelman-Camurati disease is a rare Diaphyseal dysplasia, characterized by endosteal and periostal thickness of cortex of shaft of tubular bone sparing metaphysis and epiphysis. The bone of the hand, feet, ribs, scapulae and pubis are not affected.Entities:
Mesh:
Year: 2002 PMID: 12420919 DOI: 10.1007/bf02723700
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967