Bilateral transverse (Bowdler) fibular spurs with hypophosphatasia in an adolescent girl
- PMID: 15782022
- PMCID: PMC2684999
- DOI: 10.3348/kjr.2005.6.1.52
Bilateral transverse (Bowdler) fibular spurs with hypophosphatasia in an adolescent girl
Abstract
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.
Figures

References
-
- Whyte MP. Hypophosphatasia and the role of alkaline phosphatase in skeletal mineralization. Endocr Rev. 1994;15:439–461. - PubMed
-
- States LJ. Imaging of metabolic bone disease and marrow disorders in children. Radiol Clin North Am. 2001;39:749–772. - PubMed
-
- Rathbun J. Hypophosphatasia, a new developmental anomaly. Am J Dis Child. 1948;75:822–827. - PubMed
-
- Pauli RM, Modaff P, Sipes SL, Whyte MP. Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: bent but not broken. Am J Med Genet. 1999;86:434–438. - PubMed
-
- Whyte MP, Vrabel LA, Schwartz TD. Alkaline phosphatase deficiency in cultured skin fibroblasts from patients with hypophosphatasia: comparison of the infantile, childhood, and adult forms. J Clin Endocrinol Metab. 1983;57:831–837. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources