
doi: 10.1007/bf02723700
pmid: 12420919
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.
Male, Optic Atrophy, Humans, India, Infant, Camurati-Engelmann Syndrome, Risk Assessment, Follow-Up Studies
Male, Optic Atrophy, Humans, India, Infant, Camurati-Engelmann Syndrome, Risk Assessment, Follow-Up Studies
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