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Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.
Indian J Pediatr ; 2007 Mar; 74(3): 291-3
Article in English | IMSEAR | ID: sea-80161
ABSTRACT
Ghosal type hemato-diaphyseal dysplasia is a recently described clinical entity. The authors describe such a case with severe anemia requiring transfusions and with clinical and radiological evidence of diaphyseal dysplasia. Very few such cases are reported in world literature.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Camurati-Engelmann Syndrome / Infant / Anemia Language: English Journal: Indian J Pediatr Year: 2007 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Camurati-Engelmann Syndrome / Infant / Anemia Language: English Journal: Indian J Pediatr Year: 2007 Type: Article