Osteopoikilosis: Difference between revisions
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'''Original Editor '''- | '''Original Editor '''- [[User:Tomer Yona|Tomer Yona]] <br> | ||
'''Lead Editors''' | '''Lead Editors''' | ||
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== Definition/Description == | == Definition/Description == | ||
Osteopoikilosis, also known as ‘Spotted Bone Disease’ is benign autosomal dominant bone disorder that characterised by small areas (Islands) of sclerotic bony lesions. Osteopoikilosis mainly appears in long bones, carpal and tarsal bones, the pelvis, sacrum and scapulae. | Osteopoikilosis, also known as ‘Spotted Bone Disease’ is benign autosomal dominant bone disorder that characterised by small areas (Islands) of sclerotic bony lesions. Osteopoikilosis mainly appears in long bones, carpal and tarsal bones, the pelvis, sacrum and scapulae. | ||
This disorder may appear in any ages between 15 and 60 years, with slightly more males than females affected. | This disorder may appear in any ages between 15 and 60 years, with slightly more males than females affected. | ||
The disorder is not symptomatic<ref name="hill">Hill CE, McKee L. Osteopoikilosis: An important incidental finding. Injury. 2015 Jul 1;46(7):1403-5.</ref><ref name="das">Dasgupta R, Thomas N. Spotted bone disease. BMJ case reports. 2015 May 4;2015:bcr2014208422.</ref> | The disorder is not symptomatic<ref name="hill">Hill CE, McKee L. Osteopoikilosis: An important incidental finding. Injury. 2015 Jul 1;46(7):1403-5.</ref><ref name="das">Dasgupta R, Thomas N. Spotted bone disease. BMJ case reports. 2015 May 4;2015:bcr2014208422.</ref> | ||
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== Clinical Presentation == | == Clinical Presentation == | ||
Revision as of 13:17, 24 April 2016
Original Editor - Tomer Yona
Lead Editors
Definition/Description[edit | edit source]
Osteopoikilosis, also known as ‘Spotted Bone Disease’ is benign autosomal dominant bone disorder that characterised by small areas (Islands) of sclerotic bony lesions. Osteopoikilosis mainly appears in long bones, carpal and tarsal bones, the pelvis, sacrum and scapulae.
This disorder may appear in any ages between 15 and 60 years, with slightly more males than females affected.
The disorder is not symptomatic[1][2]
Clinical Presentation[edit | edit source]
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Diagnostic Procedures[edit | edit source]
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Management / Interventions
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Differential Diagnosis
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Resources
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Case Studies[edit | edit source]
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Recent Related Research (from Pubmed)[edit | edit source]
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References[edit | edit source]
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