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Engelmann's disease with optic atrophy.
Soni, J P; Gupta, B D; Soni, M; Mund, V; Aneja, Rajesh.
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.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Optic Atrophy / Follow-Up Studies / Risk Assessment / Camurati-Engelmann Syndrome / India / Infant Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Indian J Pediatr Year: 2002 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Optic Atrophy / Follow-Up Studies / Risk Assessment / Camurati-Engelmann Syndrome / India / Infant Type of study: Etiology study / Observational study / Prognostic study / Risk factors Country/Region as subject: Asia Language: English Journal: Indian J Pediatr Year: 2002 Type: Article