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Comparative Study
. 2018 Mar;22(2):745-755.
doi: 10.1007/s00784-017-2149-4. Epub 2017 Jun 12.

Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemia

Affiliations
Comparative Study

Craniofacial and dental characteristics of patients with vitamin-D-dependent rickets type 1A compared to controls and patients with X-linked hypophosphatemia

Hans Gjørup et al. Clin Oral Investig. 2018 Mar.

Abstract

ᅟOBJECTIVES: Vitamin-D-dependent rickets type 1A (VDDR1A) is a rare inherited disease caused by defective activation of vitamin D. The aim of the study was to describe the craniofacial characteristics and the dental phenotype of patients with genetically confirmed VDDR1A. The VDDR1A findings were compared to findings in patients with X-linked hypophosphatemia (XLH) and healthy controls.

Material and methods: Ten patients with VDDR1A were identified. The reference group for the comparison of cephalometric findings was 49 adults without chronic disease. The reference group for the comparison of dental findings was 30 adults with XLH. Clinical examination, clinical photos, and radiographs were obtained. Cephalometric analysis was performed. Photos and radiographs were visually evaluated.

Results: The depth of the posterior cranial fossa (d-p and d-s-iop) in VDDR1A adults was reduced compared to the reference group (p < 0.05). Five (83%) of six adults with VDDR1A and one (4%) of 25 adults with XLH had enamel hypoplasia on several incisors and/or canines (p < 0.001). Three (75%) of four adults with VDDR1A and none of 16 adults with XLH had several first molars with enamel hypoplasia (p = 0.004). Five of 7 (71%) adults with VDDR1A and 24 of 30 (80%) adults with XLH had endodontically affected teeth.

Conclusions: The dental aberration of VDDR1A is more in line with the dental aberration of nutritional rickets than with the dental aberrations in XLH, suggesting the combination of low availability of both calcium and phosphate to be critical in periods of enamel formation.

Clinical relevance: Knowledge on craniofacial and dental aberration in patients with rare diseases, e.g., inherited rickets, is of importance to the dental practitioner, especially during diagnostics and treatment in special care units.

Keywords: Cephalometry; Craniofacial morphology; Enamel; Vitamin-D-dependent rickets type 1A; X-linked hypophosphatemia.

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References

    1. Calcif Tissue Int. 2006 Nov;79(5):294-300 - PubMed
    1. Korean J Pediatr. 2011 Feb;54(2):51-4 - PubMed
    1. Scand J Dent Res. 1994 Oct;102(5):249-53 - PubMed
    1. J Dent Res. 1979 Mar;58(Spec Issue B):1014-5 - PubMed
    1. Oral Dis. 2007 Sep;13(5):482-9 - PubMed

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