Pathological Processes in Oral Cavity at Vitamin D-Resistant Rickets (Family Case Reports)
DOI:
https://doi.org/10.56580/GEOMEDI13Keywords:
Vitamin D-resistant rickets, family case, pathological processes in the oral cavityAbstract
Vitamin D-resistant rickets of X-linked dominant transmission type is caused by pathology of renal tubular apparatus resulting in impaired absorption of calcium and phosphorus in the small intestine; it proceeds with the injuries of varying severity to skeletal system as well as dental and periodontal complex. The purpose of the study is to describe a family case of vitamin D-resistant rickets.
Metrics
References
Beck-Nielsen SS, Brusgaard K, Rasmussen LM, Brixen K, Brock-Jacobsen B, Phenotype presentation of hypophosphatemic rickets in adults.Calcif. Tissue Int. 2010 Aug;87(2):108-19.
Beltes C, Zachou E. Endodontic management in a patient with vitamin D–resistant rickets. Journal of endodontics. 2012 Feb 1;38(2):255-8.
Chu EY., Fong H., Blethen FA, Tompkins KA, Foster BL, Yeh KD, Ablation of systemic phosphate-regulating gene fibroblast growth factor 23 (Fgf23) compromises the dentoalveolar complex. Anat Rec (Hoboken). 2010 Jul;293(7):1214-26.
Endo I., Fukumoto S., Ozono K. Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatment. Endocr J. 2015;62:811–816
Faiyaz-Ul-Haque M, AlDhalaan W, AlAshwal A, et al. Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation. J Pediatr Endocrinol Metab. 2018; 31(8): 861-868.
Feldman D, J Malloy P. Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets. Bonekey Rep. 2014 Mar 5;3:510. doi: 10.1038/bonekey.2014.5. eCollection 2014.
Fong H, Chu EY, Tompkins KA, Foster BL, Sitara D, Lanske B, Somerman MJ. Aberrant cementum phenotype associated with the hypophosphatemic hyp mouse. Journal of Periodontology. 2009;80:1348–1354.
Hernández G.G., Laguna F.B. Dental characteristics of hypophosphatemic rickets. Case report Revista Odontológica Mexicana Vol. 17, No. 2 April-June 2013 pp 101- 108.
Kumar V, Kumar M, Yadav M.Alopecia in vitamin D-dependent rickets type II responding to 1α-hydroxycholecalciferol.Ann Trop Paediatr. 2010; 30(4): 329-33.
Linglart A, Biosse-Duplan M, Briot K, et al. Therapeutic management of hypophosphatemic rickets from infancy to adulthood. 2014;3(1):R13-R30
Rabbani A, Parisa R.,Vahid Ziaee and Sharareh Ghodoosi Dental Problems in Hypophosphatemic Rickets, a Cross Sectional StudyI ran J PediatrDec 2012; Vol 22 (No 4), Pp: 531-53.
Ryan JW, Anderson PH, Turner AG, Morris HA. Vitamin D activities and metabolic bone disease. Clin Chim Acta. 2013 Oct 21; 425: 148-52.
Sabandal, M. M., Robotta, P., Bürklein, S., & Schäfer, E. (2015). Review of the dental implications of X-linked hypophosphataemic rickets (XLHR). Clinical Oral Investigations, 4(19), 759-768.
Santos F., Fuente R, Mejia N., Mantecon L, Gil-Peña H, Ordoñez FA. Hypophosphatemia and growth.Pediatr Nephrol. Apr 2013;28(4):595-603.
Van Riet TC., Frank MH., Hoeben KA., de Lange J. Spontaneous dental abscesses in familial hypophosphatemic rickets. Ned Tijdschr Tandheelkd. 2012 JulAug;119(7-8):368-72
Van W.H., Hans H.U., Hypophosphatämische Rachitis Hereditäre Stoffwechselstörung und Dentin fehlbildungSchweiz Monatsschr Zahnmed Vol. 123 5/2013. 410-411.
Velásquez-Jones L., Medeiros-Domingo M., Hereditary hypophosphatemic rickets 2Bol Med Hosp Infant Mex 2013; 70(6):421-430.
Vital, S. O., Gaucher, C., Bardet, C., Rowe, P. S., George, A., Linglart, A., & Chaussain, C. (2012). Tooth dentin defects reflect genetic disorders affecting bone mineralization. Bone, 50 (4), 989-997.
Ye L, Zhang S, Ke H, Bonewald LF, Feng JQ. Periodontal breakdown in the Dmp1 null mouse model of hypophosphatemic rickets. Journal of Dental Research. 2008; 87: 624–629.
