Literature DB >> 12597691

Amelogenesis imperfecta and nephrocalcinosis: a new case of this rare syndrome.

Isabelle Normand de la Tranchade1, Hervé Bonarek, Jean-Marie Marteau, Marie-José Boileau, Javotte Nancy.   

Abstract

This article describes a new case of a rare syndrome including enamel agenesis of the primary and permanent dentition, delayed or absent eruption of the permanent dentition, coronal intra-alveolar resorption and gingival enlargement. Renal symptoms include medullary nephrocalcinosis without any apparent cause, and evolution to a renal failure. The early diagnosis provided by the oral symptoms leads to a better renal prognosis. As a consequence, pediatric dentists should be aware of this pathology.

Entities:  

Mesh:

Year:  2003        PMID: 12597691     DOI: 10.17796/jcpd.27.2.3188100w6t4516j8

Source DB:  PubMed          Journal:  J Clin Pediatr Dent        ISSN: 1053-4628            Impact factor:   1.065


  6 in total

1.  Case report: Unclassified syndrome involving dental enamel, dentine and lack of tooth eruption.

Authors:  J L Jensen; E Ambjornsen; H R Haanaes; K Storhaug
Journal:  Eur Arch Paediatr Dent       Date:  2009-12

2.  Bilateral nephrocalcinosis and amelogenesis imperfecta: A case report.

Authors:  Alok Patel; Chetana Jagtap; Chetan Bhat; Rohan Shah
Journal:  Contemp Clin Dent       Date:  2015 Apr-Jun

Review 3.  Mechanism of human tooth eruption: review article including a new theory for future studies on the eruption process.

Authors:  Inger Kjær
Journal:  Scientifica (Cairo)       Date:  2014-02-12

4.  Distal renal tubular acidosis and amelogenesis imperfecta: A rare association.

Authors:  P Ravi; T S Ekambaranath; S Ellil Arasi; E Fernando
Journal:  Indian J Nephrol       Date:  2013-11

Review 5.  Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.

Authors:  Muriel de la Dure-Molla; Mickael Quentric; Paulo Marcio Yamaguti; Ana-Carolina Acevedo; Alan J Mighell; Miikka Vikkula; Mathilde Huckert; Ariane Berdal; Agnes Bloch-Zupan
Journal:  Orphanet J Rare Dis       Date:  2014-06-14       Impact factor: 4.123

6.  FAM20A mutations can cause enamel-renal syndrome (ERS).

Authors:  Shih-Kai Wang; Parissa Aref; Yuanyuan Hu; Rachel N Milkovich; James P Simmer; Mohammad El-Khateeb; Hinda Daggag; Zaid H Baqain; Jan C-C Hu
Journal:  PLoS Genet       Date:  2013-02-28       Impact factor: 5.917

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.