Literature DB >> 19201216

Familial hypophosphatemic vitamin D-resistant rickets--prevention of spontaneous dental abscesses on primary teeth: a case report.

Diane Douyere1, Clara Joseph, Céline Gaucher, Catherine Chaussain, Frederic Courson.   

Abstract

Familial hypophosphatemic vitamin D-resistant rickets is a hereditary disease generally transmitted as an X-linked dominant trait and characterized by distinctive general clinical signs. Dental features include spontaneous dental abscesses that occur in the absence of a history of trauma or dental decay. The challenge for the dentist is to prevent and treat these lesions. This report describes the case of a young hypophosphatemic boy with abscesses. In this case, the application of fluid resin composites with a self-etching primer bonding system to all primary teeth prevented abscess formation for more than 1 year and thus avoided endodontic treatment or extraction. This constitutes a new approach to the prevention of spontaneous abscesses on primary teeth in children with familial hypophosphatemic rickets.

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Year:  2009        PMID: 19201216     DOI: 10.1016/j.tripleo.2008.12.003

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod        ISSN: 1079-2104


  8 in total

Review 1.  The rachitic tooth.

Authors:  Brian L Foster; Francisco H Nociti; Martha J Somerman
Journal:  Endocr Rev       Date:  2013-12-04       Impact factor: 19.871

Review 2.  Review of the dental implications of X-linked hypophosphataemic rickets (XLHR).

Authors:  Martin M I Sabandal; Peter Robotta; Sebastian Bürklein; Edgar Schäfer
Journal:  Clin Oral Investig       Date:  2015-02-13       Impact factor: 3.573

Review 3.  Tooth dentin defects reflect genetic disorders affecting bone mineralization.

Authors:  S Opsahl Vital; C Gaucher; C Bardet; P S Rowe; A George; A Linglart; C Chaussain
Journal:  Bone       Date:  2012-01-26       Impact factor: 4.398

4.  Dentoalveolar Abscesses Not Associated with Caries or Trauma: A Diagnostic Hallmark of Hypophosphatemic Rickets Initially Misdiagnosed as Hypochondroplasia.

Authors:  Silvia Elena Yacarini Paredes; Raquel Assed Bezerra Segato; Leila Daher Moreira; Alcides Moreira; Kranya Victoria Díaz Serrano; Clarissa Teles Rodrigues; Luciana Yamamoto Almeida; Jorge Esquiche León
Journal:  Head Neck Pathol       Date:  2017-11-30

5.  Dental management of patients with X-linked hypophosphatemia.

Authors:  Bin-Na Lee; Hye-Yoon Jung; Hoon-Sang Chang; Yun-Chan Hwang; Won-Mann Oh
Journal:  Restor Dent Endod       Date:  2017-01-06

Review 6.  Dental-craniofacial manifestation and treatment of rare diseases.

Authors:  En Luo; Hanghang Liu; Qiucheng Zhao; Bing Shi; Qianming Chen
Journal:  Int J Oral Sci       Date:  2019-02-20       Impact factor: 6.344

7.  Mineralization Defects in the Primary Dentition Associated With X-Linked Hypophosphatemic Rickets.

Authors:  Delaney Clayton; Michael B Chavez; Michelle H Tan; Tamara N Kolli; Priscila A Giovani; Kimberly J Hammersmith; Sasigarn A Bowden; Brian L Foster
Journal:  JBMR Plus       Date:  2021-03-03

8.  Therapeutic management of hypophosphatemic rickets from infancy to adulthood.

Authors:  Agnès Linglart; Martin Biosse-Duplan; Karine Briot; Catherine Chaussain; Laure Esterle; Séverine Guillaume-Czitrom; Peter Kamenicky; Jerome Nevoux; Dominique Prié; Anya Rothenbuhler; Philippe Wicart; Pol Harvengt
Journal:  Endocr Connect       Date:  2014-03-14       Impact factor: 3.335

  8 in total

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