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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Harisankar, Chidambaram Natrajan Balasubramanian, Kamleshwaran, Koramadai Karuppuswamy, Bhattacharya, Anish, Singh, Baljinder, Bhadada, Sanjay, Mittal, Bhagwant Rai
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Medknow Publications 2011
Pynciau:
Case Report
Mynediad Ar-lein: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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