1.
Indian J Pediatr
;
2002 Sep; 69(9): 823-4
Article
in English
| IMSEAR
| ID: sea-84061
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.