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.
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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