Development and Eruption of the Primary and Permanent Flashcards
________; Anomalies of number occur during this phase
• Supernumerary teeth
• Congenital tooth absence
• Initiation:
________; Anomalies of number occur during this phase
• Supernumerary teeth
• Congenital tooth absence
• Initiation:
Are supernumerary teeth more common in males or females?
Males
Syndromes with \_\_\_\_\_\_\_\_\_: Apert Cleidocranial Dysplasia Gardner syndrome Crouzon's Disease Down Syndrome Hallerman- Strief
supernumerary teeth
Is hypodontia more common in primary or permanent teeth?
Permanent
Conditions with _______:
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Ectodermal Dysplasia
Crouzon’s
Achondroplasia
Chondroectodermal Dysplasia
Ellis-van Creveld
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Hypodontia
Conditions with \_\_\_\_\_\_\_: Ectodermal dysplasia Chondroectodermal dysplasia Hemifacial microsomia Down syndrome Crouzon's
Microdontia
Conditions with: • Hemifacial hypertrophy • Crouzon's • Otodental syndrome
Macrodontia
\_\_\_\_\_\_\_\_\_: incidence 0.5%, more in primary dentition • Bifid crown with single root and pulp chamber • Familial inheritance, may impede eruption of permanent tooth, dx by counting crowns
• Gemination –
1-7.7% rare in African Americans, maxillary lateral most often, both dentitions, etiology is invagination of inner enamel epithelium, clinical significance is caries related
• Dens in dente (Invaginatus):
• Incidence – 1-4%, caused by evagination of enamel
epithelium focal hyperplasia of pulp mesenchyme
• Significance – pulp tissue in cusp may complicate
restorations
Dents evaginatus – Talon Cusp
Failure of proper invagination of Hertwig’s epithelial root sheath; incidence - .54-5.6%, higher in patients with hypophosphatemic rickets Syndromes – Klinefelter, Trichodento-osseous, Orofacialdigital, Ectodermal dysplasia, Amelogenesis imperfecta Type IV, Down
Taurodontism
• Usually due to trauma in
primary dentition
• Lamellar ichthyosis –
syndrome associated
Dilaceration
• Inherited defect with multiple patterns such as X-linked, Autosomal dominant or recessive • Incidence variable from 1:14,000 to 1:4000 • 4 major types with 14 subgroups • Distinguished from other enamel defects because of inheritance and no syndrome or systemic disease
• Amelogenesis Imperfecta
Heritable defect of predentin matrix;normal mantle dentin Incidence 1:8000 Shields Type I – occurs with Osteogenesis Imperfecta Shields Type II – “opalescent dentin”, occurs alone, both dentitions affected Shields Type III – most severe with several variants
Dentinogenesis