UID:
almahu_9948026386202882
Format:
1 online resource (265 p.)
Edition:
1st ed.
ISBN:
1-280-58240-5
,
9786613612182
,
0-12-391473-6
Series Statement:
Elsevier insights
Content:
Dental defects may be the physical expression of genetic defects, and so they can often be seen in a variety of syndromes associated with malformations of organs. However, dental defects are often not recognized, identified, nor characterised despite representing a possible diagnostic sign for an undiagnosed condition. This book addresses this gap by providing an understanding of dental genetics and its developmental biology counterpart. With approximately seventy well-illustrated examples, the authors present the clinical oro-facial manifestations accompanying various syndromes, providing
Note:
Description based upon print version of record.
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Front Cover; Dento/Oro/Craniofacial Anomalies and Genetics; Copyright Page; Contents; Foreword; Acknowledgments; Introduction; 1 Odontogenesis, Anomalies and Genetics; 1.1 Odontogenesis; 1.1.1 Tooth Development; 1.1.2 Developing Through Epithelio-mesenchymal Interactions with Signalling Molecules and Transcription Factors; 1.1.3 Signalling Pathways; Initiation Stage; Placode Formation; Bud-to-Cap Stage Transition; Bell Stage; Cell Differentiations; Eruption; 1.2 Dental Anomalies; 1.3 Syndromes and Dental Anomalies; 2 Missing Teeth (Hypodontia and Oligodontia); 2.1 Transcription Factors
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2.1.1 MSX1 Hypodontia and OligodontiaDefinition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical Description; Management/Oral Health; References; Pictures Illustrating the Oro-Dental Features; 2.1.2 Witkop Syndrome; Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical Description; References; Pictures Illustrating the Oro-Dental Features; 2.1.3 Wolf-Hirschhorn Syndrome; Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene (4p-)
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Animal Models/Main FeaturesClinical Description; References; Pictures Illustrating the Oro-Dental Features; 2.1.4 PAX9 Hypodontia and Oligodontia; Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical description; Management/Oral Health; References; Pictures Illustrating the Oro-Dental Features; 2.1.5 Axenfeld-Rieger Syndrome (Rieger Syndrome); Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene [182-188]; Animal Models/Main Features; Clinical Description; References
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Pictures Illustrating the Oro-Dental Features2.2 WNT Signalling Pathway; 2.2.1 Oligodontia and Colorectal Cancer Syndrome; Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical Description; Management/Oral Health; References; Pictures Illustrating the Oro-Dental Features; 2.2.2 Odonto-Onycho-Dermal Dysplasia (OODD); Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical Description; References; Pictures Illustrating the Oro-Dental Features
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2.3 TNF/NF-Kappa B Signalling Pathway2.3.1 Hypohidrotic Ectodermal Dysplasia (HED); Definition; OMIM Number; Prevalence; Inheritance [218-220]; Aetiology - Molecular Basis - Gene [221-225]; Animal Models/Main Features; Clinical Description; Management/Oral Health [235-239]; References; Pictures Illustrating the Oro-Dental Features; 2.3.2 Hypohidrotic Ectodermal Dysplasia with Immune Deficiency (HED-ID); Definition; OMIM Number; Prevalence; Inheritance; Aetiology - Molecular Basis - Gene; Animal Models/Main Features; Clinical Description; Management/Oral Health; References
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2.3.3 Incontinentia Pigmenti
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English
Additional Edition:
ISBN 0-12-416038-7
Language:
English
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