American Journal of Clinical Medicine Research
ISSN (Print): 2328-4005 ISSN (Online): 2328-403X Website: http://www.sciepub.com/journal/ajcmr Editor-in-chief: Dario Galante
Open Access
Journal Browser
Go
American Journal of Clinical Medicine Research. 2014, 2(4), 68-71
DOI: 10.12691/ajcmr-2-4-1
Open AccessCase Report

Orofacial and Skeletal Manifestations of Hypophosphatemic Rickets in Fanconi Bickel Syndrome

Veena R1, Babitha. K2, 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

Pub. Date: July 31, 2014

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

Creative CommonsThis 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/

References:

[1]  Golembiewska E and Ciechanowski K. Renal tubular acidosis-underrated problem? Acta biochimica polonica. 2012; 59 (2).
 
[2]  Deshpande P and Ali U. Primary Fanconi Syndrome. Indian pediatrics 1997; 34: 547-49.
 
[3]  Setoodeh A and Rabbani A. Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome. Acta Medica Iranica 2012; 50 (12) 837
 
[4]  Hadipour F et al. Fanconi syndrome versus osteogenesis imperfecta: An Iranian case with novel gene mutation in glucose transporter 2 gene and review of literature. Indian journal of human genetics. 2013; 19 (1): 84-86.
 
[5]  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.
 
[6]  Jagtap s v. et al. review: Hypophosphatemic rickets. Indian journal of endocrinology and metabolism. 2012; 16 (2) 177-182.
 
[7]  Puneet Batra, Zahra Tejani, Michael Mars, X-Linked hypophosphatemia: Dental and histologic findings J Can Dent Assoc 2006; 72 (1): 69-72.
 
[8]  Savelli PD et al: Fanconi syndrome. Metabolic studies on treatment. The Journal of bone and joint surgery. 1955; 37 (4) 529-539.
 
[9]  James C.M. Chan, Jon I. Scheinman, Karl S. Roth Renal Tubular Acidosis. Pediatrics in Review Vol.22 No.8 August 2001. 277-87.
 
[10]  Tümen et al. Types of Rickets, Dental and Histologic Findings: Review of the Literature. Pesq Bras Odontoped Clin Integr, João Pessoa 2009 9 (2): 241-246
 
[11]  Pereira et al Dental Alterations Associated with X-Linked hypophosphatemic rickets. Journal of Endodontics 2004; 30 (4) 241-45.
 
[12]  Aysun Avsar: Dental findings in a child with glycogen storage disease type IA. Quintessence international 2007 ; 37: e36-e40
 
[13]  Antieevie D et al,osteogenesis imperfecta: A current overview of musculskeletal radiology and new genetic concepts. Acta Clin Croat 2002; 41 (Suppl): 101-111.
 
[14]  Ravi Prakash S. Mohan. Cleidocranial dysplasia: Clinic radiological illustration of a rare case Journal of Oral Science, Vol. 52, No. 1, 161-166, 2010.
 
[15]  Smriti Rohilla Case report: Orofacial manifestations of achondroplasia EXCLI Journal 2012; 11: 538-542.