Literature DB >> 3163135

Autosomal recessive rough hypoplastic amelogenesis imperfecta. A case report with clinical, light microscopic, radiographic, and electron microscopic observations.

K Ooya1, J Nalbandian, T Noikura.   

Abstract

A case is presented of a 12-year-old Japanese girl with nearly complete lack of enamel in the deciduous and the permanent dentitions, coupled with a gross abnormality in the pattern of eruption. There was no family history of a similar condition. Deciduous molars were extracted, and hyperplastic gingival tissue was resected. On the basis of clinical, radiographic, and microscopic findings, a diagnosis of autosomal recessive rough hypoplastic amelogenesis imperfecta was made. The configuration of the abnormal enamel was examined with scanning and transmission electron microscopy as well as with light microscopy. Prismatic structure was virtually absent, and the scant enamel showed globular protrusions superficially. Two different surface structures were identified as covering parts of the enamel. At the ultrastructural level, calcified bodies located in the gingival tissue appeared to be composed, in part, of a dense enamel-like substance and, in part, of a tissue with features of afibrillar cementum.

Entities:  

Mesh:

Year:  1988        PMID: 3163135     DOI: 10.1016/0030-4220(88)90360-x

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN: 0030-4220


  10 in total

1.  Amelogenesis imperfecta associated with dental follicular-like hamartomas and generalised gingival enlargement.

Authors:  S O'Connell; J Davies; J Smallridge; M Vaidyanathan
Journal:  Eur Arch Paediatr Dent       Date:  2013-12-19

2.  Case series: clinical findings and oral rehabilitation of patients with amelogenesis imperfecta.

Authors:  D Markovic; B Petrovic; T Peric
Journal:  Eur Arch Paediatr Dent       Date:  2010-08

3.  Multidisciplinary approach for restoring function and esthetics in a patient with amelogenesis imperfecta: a clinical report.

Authors:  Vaibhav D Kamble; Rambhau D Parkhedkar
Journal:  J Clin Diagn Res       Date:  2013-12-15

4.  Restoring Function and Aesthetics in a Class II Division 1 Patient with Amelogenesis Imperfecta: A Clinical Report.

Authors:  Cenk Doruk; Firat Ozturk; Fatih Sari; Mehmet Turgut
Journal:  Eur J Dent       Date:  2011-04

5.  Amelogenesis imperfecta: Report of a case and review of literature.

Authors:  Mayur Chaudhary; Shweta Dixit; Asha Singh; Sanket Kunte
Journal:  J Oral Maxillofac Pathol       Date:  2009-07

6.  Restoring aesthetics and function in a young boy with hypomature amelogenesis imperfecta: a case report.

Authors:  Engin Ağaçkiran; Emin Caner Tümen; Sema Celenk; Behiye Bolgül; Fatma Atakul
Journal:  ISRN Dent       Date:  2010-09-21

7.  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 8.  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

9.  Amelogenesis imperfecta and generalized gingival overgrowth resembling hereditary gingival fibromatosis in siblings: a case report.

Authors:  Emre Yaprak; Meryem Gülce Subaşı; Mustafa Avunduk; Filiz Aykent
Journal:  Case Rep Dent       Date:  2012-10-09

10.  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

  10 in total

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