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Şimşek E, et al Case report: A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome The Turkish Journal of Pediatrics 2009; 51: 166-168.

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Article

Orofacial and Skeletal Manifestations of Hypophosphatemic Rickets in Fanconi Bickel Syndrome

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


American Journal of Clinical Medicine Research. 2014, Vol. 2 No. 4, 68-71
DOI: 10.12691/ajcmr-2-4-1
Copyright © 2014 Science and Education Publishing

Cite this paper:
Veena R, Babitha. K, 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.

Correspondence to: Babitha.  K, Post graduate student in department of oral medicine & radiology, The Oxford dental college, Bommanahalli, Hosur road, Bangalore 560068, Karnataka, India. Email: dr.babitha.k@gmail.com

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.

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