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Fibrodysplasia Ossificans Progressiva - A Rare Genetic Disorder and the Role of Technetium-99m Methylene Diphosphonate Bone Scan.

Authors :
Gupta, Nitin
Pruthi, Ankur
Kumar, Suneel
Verma, Ritu
Belho, Ethel Shangne
Source :
Indian Journal of Nuclear Medicine. Jul-Sep2019, Vol. 34 Issue 3, p209-212. 4p.
Publication Year :
2019

Abstract

Fibrodysplasia ossificans progressiva is a rare genetic disease believed to occur in approximately 1 in 2 million people worldwide and is characterized by progressive extraosseous ossification over the course of a lifetime in an inevitable and unpredictable episodic manner, with most patients being confined to a wheelchair by the third decade of life and requiring life-long care. The extraosseous calcification involves ligaments, tendons, muscles, and connective tissue leading to severe restriction of movements. Another hallmark of this condition is abnormal great toes. The diagnosis is often made on clinical and radiological examination, but Technetium-99m methylene diphosphonate (Tc-99m MDP) bone scan is usually indicated to determine the extent of the disease. We hereby present a case series comprising of four patients suffering from this debilitating illness who underwent Tc99m MDP bone scan for initial diagnosis and localizing sites of heterotopic ossification. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09723919
Volume :
34
Issue :
3
Database :
Academic Search Index
Journal :
Indian Journal of Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
137105853
Full Text :
https://doi.org/10.4103/ijnm.IJNM_57_19