Orofacial and Skeletal Manifestations of Hypophosphatemic Rickets in Fanconi Bickel Syndrome

Veena R¹, Babitha. K^2, and Anuradha Pai³

¹Reader in department of oral medicine & radiology, The Oxford dental college, Bommanahalli, Hosur road, Bangalore 560068, Karnataka, India

²Post graduate student in department of oral medicine & radiology, The Oxford dental college, Bommanahalli, Hosur road, Bangalore 560068, Karnataka, India

³Professor and head of the department of oral medicine & radiology, The Oxford dental college, Bommanahalli, Hosur road, Bangalore 560068, Karnataka, India

Cite this paper

Veena R, Babitha. K and Anuradha Pai. Orofacial and Skeletal Manifestations of Hypophosphatemic Rickets in Fanconi Bickel Syndrome. American Journal of Clinical Medicine Research. 2014; 2(4):68-71. doi: 10.12691/AJCMR-2-4-1

Abstract

Wide array of systemic disorders have their manifestations in oral cavity. These disorders can be mainly syndromic, metabolic or congenital diseases. The dental features in these disorders can be expressed on a wider latitude from mild to extensive forms. Here is an incidence of a case of hypophosphatemic rickets in Fanconi Bickel syndrome with multiple oral and general phenotypic features.

Keywords

Fanconi syndrome, hypophosphatemic rickets, oligodontia

Copyright

This work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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