Literature DB >> 28043400

Dental issues in lacrimo-auriculo-dento-digital syndrome: An autosomal dominant condition with clinical and genetic variability.

M J Hajianpour, Hannah Bombei, Scott M Lieberman, Rachael Revell, Rachana Krishna, Robert Gregorsok, Simon Kao, Jeff M Milunsky.   

Abstract

BACKGROUND AND OVERVIEW: Lacrimo-auriculo-dento-digital (LADD) syndrome is an autosomal dominant disorder with variable lacrimal and salivary gland hypoplasia and aplasia, auricular anomalies and hearing loss, dental defects and caries, and digital anomalies. CASE DESCRIPTION: The authors present the cases of 2 unrelated children with enamel defects and history of dry mouth leading to recurrent dental caries. The referring diagnoses were Sjögren disease and hypohidrotic ectodermal dysplasia, respectively. The geneticist suspected LADD syndrome, which was confirmed by means of molecular studies showing mutations of 2 genes: fibroblast growth factor receptor 2 and fibroblast growth factor 10, respectively. Similarly affected relatives indicated an autosomal dominant inheritance. These relatives needed multiple dental rehabilitations during childhood and dentures in adulthood. CONCLUSIONS AND PRACTICAL IMPLICATIONS: Dry mouth, multiple caries, enamel defects, and abnormal tooth morphology were the reasons for seeking care from dentists. However, clinical evaluation and diagnostic imaging studies helped identify anomalies of the lacrimal and salivary glands, ears, and digits, indicating involvement of different areas of the body, compatible with LADD syndrome. Accordingly, dentists should consider genetic disorders in patients with multiple anomalies. For instance, oculodentodigital syndrome, oral-facial-digital syndrome, and LADD syndrome (among others) may have dental issues as the major clinical manifestation. Accurate identification of a particular syndrome is now commonplace with the use of genetic testing. When a patient has multiple anomalies suggestive of a syndromic condition, appropriate genetic testing can help verify the clinical diagnosis. Keeping genetics in mind helps earlier identification of other affected family members with diagnostic genetic testing and appropriate treatment; the economic advantage is to shorten the diagnostic odyssey and possibly preserve dentition.
Copyright © 2017 American Dental Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dental enamel; Sjögren disease; caries; genetics; salivary glands

Mesh:

Year:  2016        PMID: 28043400     DOI: 10.1016/j.adaj.2016.11.016

Source DB:  PubMed          Journal:  J Am Dent Assoc        ISSN: 0002-8177            Impact factor:   3.634


  2 in total

Review 1.  Lacrimo-auriculo-dento-digital syndrome: A novel mutation in a Korean family and review of literature.

Authors:  Young Hye Ryu; Jong Kyun Chae; Jung-Wook Kim; Soyoung Lee
Journal:  Mol Genet Genomic Med       Date:  2020-07-26       Impact factor: 2.183

Review 2.  Bilateral parotid glands aplasia: a case report and literature review.

Authors:  Hojka Kuralt; Aleš Fidler; Ana Blatnik; Srdjan Novaković; Gaber Plavc
Journal:  Oral Radiol       Date:  2022-01-25       Impact factor: 1.882

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.