Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease

Engelmann-Camurati disease (ECD) is a rare bone disorder characterized by autosomal dominant inheritance. It usually presents in early childhood and is associated with symmetrical diaphyseal sclerosis. We report a 20-year-old female with scintigraphic findings characteristic of ECD. She was treated...

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Bibliografiset tiedot
Päätekijät: Harisankar, Chidambaram Natrajan Balasubramanian, Kamleshwaran, Koramadai Karuppuswamy, Bhattacharya, Anish, Singh, Baljinder, Bhadada, Sanjay, Mittal, Bhagwant Rai
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Medknow Publications 2011
Aiheet:
Case Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3180724/
https://ncbi.nlm.nih.gov/pubmed/21969782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-3919.84615
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