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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.


Subject(s)
Camurati-Engelmann Syndrome/complications , Follow-Up Studies , Humans , India , Infant , Male , Optic Atrophy/complications , Risk Assessment
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