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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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Autores principales: Harisankar, Chidambaram Natrajan Balasubramanian, Kamleshwaran, Koramadai Karuppuswamy, Bhattacharya, Anish, Singh, Baljinder, Bhadada, Sanjay, Mittal, Bhagwant Rai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180724/
https://www.ncbi.nlm.nih.gov/pubmed/21969782
http://dx.doi.org/10.4103/0972-3919.84615
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author Harisankar, Chidambaram Natrajan Balasubramanian
Kamleshwaran, Koramadai Karuppuswamy
Bhattacharya, Anish
Singh, Baljinder
Bhadada, Sanjay
Mittal, Bhagwant Rai
author_facet Harisankar, Chidambaram Natrajan Balasubramanian
Kamleshwaran, Koramadai Karuppuswamy
Bhattacharya, Anish
Singh, Baljinder
Bhadada, Sanjay
Mittal, Bhagwant Rai
author_sort Harisankar, Chidambaram Natrajan Balasubramanian
collection PubMed
description 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 with corticosteroids and showed marked clinical improvement.
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spelling pubmed-31807242011-10-03 Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease Harisankar, Chidambaram Natrajan Balasubramanian Kamleshwaran, Koramadai Karuppuswamy Bhattacharya, Anish Singh, Baljinder Bhadada, Sanjay Mittal, Bhagwant Rai Indian J Nucl Med Case Report 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 with corticosteroids and showed marked clinical improvement. Medknow Publications 2011 /pmc/articles/PMC3180724/ /pubmed/21969782 http://dx.doi.org/10.4103/0972-3919.84615 Text en Copyright: © Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Harisankar, Chidambaram Natrajan Balasubramanian
Kamleshwaran, Koramadai Karuppuswamy
Bhattacharya, Anish
Singh, Baljinder
Bhadada, Sanjay
Mittal, Bhagwant Rai
Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title_full Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title_fullStr Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title_full_unstemmed Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title_short Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
title_sort tc99m-mdp bone scintigraphy in engelmann-camurati disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180724/
https://www.ncbi.nlm.nih.gov/pubmed/21969782
http://dx.doi.org/10.4103/0972-3919.84615
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