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Dental issues in lacrimo-auriculo-dento-digital syndrome: An autosomal dominant condition with clinical and genetic variability.
- Source :
-
Journal of the American Dental Association (1939) [J Am Dent Assoc] 2017 Mar; Vol. 148 (3), pp. 157-163. Date of Electronic Publication: 2016 Dec 30. - Publication Year :
- 2017
-
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.<br />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.<br />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.<br /> (Copyright © 2017 American Dental Association. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Child
Child, Preschool
Diagnosis, Differential
Female
Humans
Male
Mutation
Pedigree
Abnormalities, Multiple diagnosis
Abnormalities, Multiple genetics
Dental Care for Children
Dental Care for Chronically Ill
Hearing Loss diagnosis
Hearing Loss genetics
Lacrimal Apparatus Diseases diagnosis
Lacrimal Apparatus Diseases genetics
Syndactyly diagnosis
Syndactyly genetics
Tooth Abnormalities diagnosis
Tooth Abnormalities genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1943-4723
- Volume :
- 148
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of the American Dental Association (1939)
- Publication Type :
- Academic Journal
- Accession number :
- 28043400
- Full Text :
- https://doi.org/10.1016/j.adaj.2016.11.016