Access the full text.
Sign up today, get DeepDyve free for 14 days.
Doron Bresler, J. Bruder, K. Mohnike, W. Fraser, P. Rowe (2004)
Serum MEPE-ASARM-peptides are elevated in X-linked rickets (HYP): implications for phosphaturia and rickets.The Journal of endocrinology, 183 3
C. Chaussain-Miller, C. Sinding, M. Wolikow, J. Lasfargues, G. Godeau, M. Garabédian (2003)
Dental abnormalities in patients with familial hypophosphatemic vitamin D-resistant rickets: prevention by early treatment with 1-hydroxyvitamin D.The Journal of pediatrics, 142 3
P. Rowe, Y. Kumagai, G. Gutierrez, I. Garrett, R. Blacher, D. Rosen, J. Cundy, S. Navvab, Di Chen, M. Drezner, L. Quarles, G. Mundy (2004)
MEPE has the properties of an osteoblastic phosphatonin and minhibin.Bone, 34 2
Sonia Balsan, Martin Tieder (1990)
Linear growth in patients with hypophosphatemic vitamin D-resistant rickets: influence of treatment regimen and parental height.The Journal of pediatrics, 116 3
R. D'Souza, A. Bronckers, R. Happonen, D. Doga, M. Farach-Carson, W. Butler (1992)
Developmental expression of a 53 KD dentin sialoprotein in rat tooth organs.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 40
P. Rowe, I. Garrett, P. Schwarz, D. Carnes, E. Lafer, G. Mundy, G. Gutierrez (2005)
Surface plasmon resonance (SPR) confirms that MEPE binds to PHEX via the MEPE-ASARM motif: a model for impaired mineralization in X-linked rickets (HYP).Bone, 36 1
L. Fisher, N. Fedarko (2003)
Six Genes Expressed in Bones and Teeth Encode the Current Members of the SIBLING Family of ProteinsConnective Tissue Research, 44
T. Murayama, R. Iwatsubo, S. Akiyama, A. Amano, I. Morisaki (2000)
Familial hypophosphatemic vitamin D-resistant rickets: dental findings and histologic study of teeth.Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics, 90 3
G. Hunter, H. Goldberg (1994)
Modulation of crystal formation by bone phosphoproteins: role of glutamic acid-rich sequences in the nucleation of hydroxyapatite by bone sialoprotein.The Biochemical journal, 302 ( Pt 1)
F. Francis, S. Hennig, B. Korn, R. Reinhardt, P. Jong, A. Poustka, H. Lehrach, P. Rowe, J. Goulding, T. Summerfield, R. Mountford, A. Read, E. Popowska, E. Pronicka, K. Davies, J. O'riordan, Michael Econs, T. Nesbitt, M. Drezner, C. Oudet, S. Pannetier, A. Hanauer, T. Strom, A. Meindl, Birgit Lorenz, B. Cagnoli, K. Mohnike, J. Murken, T. Meitinger (1995)
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic ricketsNature Genetics, 11
O. Mäkitie, A. Doria, S. Kooh, W. Cole, A. Daneman, E. Sochett (2003)
Early treatment improves growth and biochemical and radiographic outcome in X-linked hypophosphatemic rickets.The Journal of clinical endocrinology and metabolism, 88 8
T. Nesbitt, I. Fujiwara, Ronald Thomas, Zhou-sheng Xiao, L. Quarles, M. Drezner (1999)
Coordinated Maturational Regulation of PHEX and Renal Phosphate Transport Inhibitory Activity: Evidence for the Pathophysiological Role of PHEX in X‐Linked HypophosphatemiaJournal of Bone and Mineral Research, 14
Narayanan Narayanan, Ramachandran Ramachandran, Hao Hao (2003)
Dual functional roles of dentin matrix protein 1. Implications in biomineralization and gene transcription by activation of intracellular Ca2+ storeJ Biol Chem, 278
Goodman Goodman, Gelbier Gelbier, Bennett Bennett, Winter Winter (1998)
Dental problems associated with hypophosphatemic vitamin D‐resistant ricketsInt J Pediatr Dent, 8
Peter Rowe, C. Oudet, Fiona Francis, Christiane Sinding, S. Pannetier, Mike Econs, Tim Strom, T. Meitinger, Michèle Garabédian, Albert David, Marie-Alice Macher, Elisabeth Questiaux, E. Popowska, E. Pronicka, A. Read, Agnes Mokrzycki, F. Glorieux, M. Drezner, Andr Hanauer, Hans Lehrach, J. Goulding, J.L.H. O'Riordan (1997)
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).Human molecular genetics, 6 4
W. Seow, H. Needleman, I. Holm (1995)
Effect of familial hypophosphatemic rickets on dental development: a controlled, longitudinal study.Pediatric dentistry, 17 5
A. Bronckers, P. Price, A. Schrijvers, T. Bervoets, G. Karsenty (1998)
Studies of osteocalcin function in dentin formation in rodent teeth.European journal of oral sciences, 106 3
M. Vaisbich, V. Koch (2006)
Hypophosphatemic rickets: results of a long-term follow-upPediatric Nephrology, 21
K. Jonsson, R. Zahradnik, T. Larsson, K. White, T. Sugimoto, Y. Imanishi, Takehisa Yamamoto, G. Hampson, H. Koshiyama, O. Ljunggren, K. Oba, I. Yang, A. Miyauchi, M. Econs, J. Lavigne, H. Jüppner (2003)
Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia.The New England journal of medicine, 348 17
T. Onishi, T. Ogawa, T. Hayashibara, T. Hoshino, R. Okawa, T. Ooshima (2005)
Hyper-expression of Osteocalcin mRNA in Odontoblasts of Hyp MiceJournal of Dental Research, 84
J. Jernvall, Han-Sung Jung, Han-Sung Jung (2000)
Genotype, phenotype, and developmental biology of molar tooth characters.American journal of physical anthropology, Suppl 31
P. Rowe (2004)
The wrickkened pathways of FGF23, MEPE and PHEX.Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists, 15 5
R. Wang, Stephen Weiner (1997)
Strain-structure relations in human teeth using Moiré fringes.Journal of biomechanics, 31 2
S. Miard, R. Peterkova, J. Vonesch, M. Peterka, J. Ruch, H. Lesot (1999)
Alterations in the incisor development in the Tabby mouse.The International journal of developmental biology, 43 6
M. Goldberg, D. Septier, K. Bourd, R. Hall, J. Jeanny, L. Jonet, S. Colin, F. Tager, C. Chaussain-Miller, M. Garabédian, A. George, H. Goldberg, S. Ménashi (2002)
The Dentino-Enamel Junction RevisitedConnective Tissue Research, 43
P. Ducy, C. Desbois, B. Boyce, G. Pinero, B. Story, C. Dunstan, Erica Smith, J. Bonadio, S. Goldstein, C. Gundberg, A. Bradley, G. Karsenty (1996)
Increased bone formation in osteocalcin-deficient miceNature, 382
J. Goodman, M. Gelbier, J. Bennett, G. Winter (1998)
Dental problems associated with hypophosphataemic vitamin D resistant rickets.International journal of paediatric dentistry, 8 1
N. Friedman, B. Lobaugh, M. Drezner (1993)
Effects of calcitriol and phosphorus therapy on the growth of patients with X-linked hypophosphatemia.The Journal of clinical endocrinology and metabolism, 76 4
C. Qin, O. Baba, W. Butler (2004)
Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis.Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists, 15 3
Chaussain‐Miller Chaussain‐Miller, Sinding Sinding, Wolikow Wolikow, Lasfargues Lasfargues, Garabedian Garabedian (2003)
Dental abnormalities in patients with X‐linked hypophosphatemic rickets: prevention by early treatment with 1‐hydroxyvitamin DJ Pediatr, 142
Shiguang Liu, T. Brown, Jianping Zhou, Zhou-sheng Xiao, H. Awad, F. Guilak, L. Quarles (2005)
Role of matrix extracellular phosphoglycoprotein in the pathogenesis of X-linked hypophosphatemia.Journal of the American Society of Nephrology : JASN, 16 6
K. Narayanan, A. Ramachandran, J. Hao, G. He, Ky Park, M. Cho, A. George (2003)
Dual Functional Roles of Dentin Matrix Protein 1The Journal of Biological Chemistry, 278
K. Abe, Takashi Ooshima, Y. Masatomi, S. Sobue, Yutaka Moriwaki (1989)
Microscopic and Crystallographic Examinations of the Teeth of the X-linked Hypophosphatemic MouseJournal of Dental Research, 68
Objective: To evaluate the outcome of 1‐(OH) vitamin D and oral phosphate treatment on dentin structure in patients with familial hypophosphatemic rickets, and expression of SIBLINGs (a family of non‐collagenous proteins involved in dentinogenesis) and osteocalcin. Patients and methods: Seven patients with familial hypophosphatemic rickets (age 3–16 years) were studied before or during treatment. Deciduous and permanent teeth were prepared for scanning electron microscopy (SEM) analysis and immunohistochemistry. Results: Untreated or inadequately treated patients had necrotic teeth with impaired dentin mineralization including unmerged calcospherites and accumulation of non‐collagenous proteins in wide interglobular spaces. Most of the primary incisors analyzed displayed fissures linking enamel subsurface to pulp horn. These elements may explain the bacterial penetration and dental abscesses despite the absence of carious lesions. Well‐treated patients had healthy teeth with good dentin mineralization and little evidence of calcospherites. Conclusion: Treatment of hypophosphatemic children with 1‐(OH) vitamin D and oral phosphate insures good dentin development and mineralization, and prevents clinical anomalies such as the dental necrosis classically associated with the disease. Starting treatment during early childhood and good adherence to the therapy are mandatory to observe these beneficial effects.
Oral Diseases – Wiley
Published: Sep 1, 2007
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.