| Literature DB >> 6461731 |
M M Lundy, J L Billingsley, M D Redwine, G L Turnbull, T J Brown.
Abstract
A 14-yr-old white male with a severe form of progressive diaphyseal dysplasia (Engelmann-Camurati disease) was referred to our institution for evaluation of splenomegaly, which is not usually associated with the disease. Our studies included bone-marrow, and liver-spleen scans. These scintigraphic findings, along with the probable cause for splenomegaly, are discussed.Entities:
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Year: 1982 PMID： 6461731
Source DB: PubMed Journal: J Nucl Med ISSN： 0161-5505 Impact factor: 10.057