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Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl
Hypophosphatasia is a clinically heterogeneous inheritable disorder characterized by defective bone mineralization and the deficiency of serum and tissue liver/bone/kidney alkaline phosphatase activities. Due to the mineralization defect of the bones, various skeletal findings can be radiologically...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Radiological Society
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684999/ https://www.ncbi.nlm.nih.gov/pubmed/15782022 http://dx.doi.org/10.3348/kjr.2005.6.1.52 |
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author | Uras, Ismail Uras, Nurdan Karadag, Ahmet Yavuz, Osman Yuksel Atalar, Hakan |
author_facet | Uras, Ismail Uras, Nurdan Karadag, Ahmet Yavuz, Osman Yuksel Atalar, Hakan |
author_sort | Uras, Ismail |
collection | PubMed |
description | Hypophosphatasia is a clinically heterogeneous inheritable disorder characterized by defective bone mineralization and the deficiency of serum and tissue liver/bone/kidney alkaline phosphatase activities. Due to the mineralization defect of the bones, various skeletal findings can be radiologically observed in hypophosphatasia. Bowing and Bowdler spurs of long bones are the characteristic findings. The Bowdler spurs reported on in the previous pertinent literature were observed in the perinatal aged patients and these lesions have rarely involved adolescents. We herein report on a 14-year-old girl with fibular Bowdler spurs. |
format | Text |
id | pubmed-2684999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Korean Radiological Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-26849992009-05-29 Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl Uras, Ismail Uras, Nurdan Karadag, Ahmet Yavuz, Osman Yuksel Atalar, Hakan Korean J Radiol Case Report Hypophosphatasia is a clinically heterogeneous inheritable disorder characterized by defective bone mineralization and the deficiency of serum and tissue liver/bone/kidney alkaline phosphatase activities. Due to the mineralization defect of the bones, various skeletal findings can be radiologically observed in hypophosphatasia. Bowing and Bowdler spurs of long bones are the characteristic findings. The Bowdler spurs reported on in the previous pertinent literature were observed in the perinatal aged patients and these lesions have rarely involved adolescents. We herein report on a 14-year-old girl with fibular Bowdler spurs. The Korean Radiological Society 2005 2005-03-31 /pmc/articles/PMC2684999/ /pubmed/15782022 http://dx.doi.org/10.3348/kjr.2005.6.1.52 Text en Copyright © 2005 The Korean Radiological Society http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Uras, Ismail Uras, Nurdan Karadag, Ahmet Yavuz, Osman Yuksel Atalar, Hakan Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title | Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title_full | Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title_fullStr | Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title_full_unstemmed | Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title_short | Bilateral Transverse (Bowdler) Fibular Spurs with Hypophosphatasia in an Adolescent Girl |
title_sort | bilateral transverse (bowdler) fibular spurs with hypophosphatasia in an adolescent girl |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684999/ https://www.ncbi.nlm.nih.gov/pubmed/15782022 http://dx.doi.org/10.3348/kjr.2005.6.1.52 |
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