Development and Eruption of the Primary and Permanent Flashcards

1
Q

________; Anomalies of number occur during this phase
• Supernumerary teeth
• Congenital tooth absence

A

• Initiation:

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1
Q

________; Anomalies of number occur during this phase
• Supernumerary teeth
• Congenital tooth absence

A

• Initiation:

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2
Q

Are supernumerary teeth more common in males or females?

A

Males

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3
Q
Syndromes with 
\_\_\_\_\_\_\_\_\_:
Apert Cleidocranial 
Dysplasia
Gardner 
syndrome
Crouzon's 
Disease
Down 
Syndrome
Hallerman-
Strief
A

supernumerary teeth

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4
Q

Is hypodontia more common in primary or permanent teeth?

A

Permanent

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5
Q

Conditions with _______:

```
Ectodermal Dysplasia
Crouzon’s
Achondroplasia
Chondroectodermal Dysplasia
Ellis-van Creveld
~~~

A

Hypodontia

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6
Q
Conditions with \_\_\_\_\_\_\_:         
Ectodermal dysplasia
Chondroectodermal dysplasia
Hemifacial microsomia
Down syndrome
Crouzon's
A

Microdontia

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7
Q
Conditions with:
• Hemifacial 
hypertrophy
• Crouzon's
• Otodental 
syndrome
A

Macrodontia

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8
Q
\_\_\_\_\_\_\_\_\_:
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
A

• Gemination –

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9
Q
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
A

• Dens in dente (Invaginatus):

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10
Q

• Incidence – 1-4%, caused by evagination of enamel
epithelium focal hyperplasia of pulp mesenchyme
• Significance – pulp tissue in cusp may complicate
restorations

A

Dents evaginatus – Talon Cusp

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11
Q
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
A

Taurodontism

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12
Q

• Usually due to trauma in
primary dentition
• Lamellar ichthyosis –
syndrome associated

A

Dilaceration

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13
Q
• 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
A

• Amelogenesis Imperfecta

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14
Q
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
A

Dentinogenesis

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15
Q

Anomalies of __________:
• Dentin dysplasia – Shields type I and II
• Regional odontodysplasia – “ghost teeth”
• Other conditions associated with dentin abnormalities –
vit-D resistant Rickets, hypoparathyroidism, Albright’s,
Ehlers-Danlos, Epidermolysis Bullosa, Osteogenesis
imperfecta

A

Dentin

Apposition

16
Q

Anomalies of ________:
• Hypercementosis
• Hypophosphotasia:

A

Apposition -

Cementum

17
Q

_________– prevalence is 4-70%
from European studies
• Possible problem with ameloblast function after full
matrix completion
• May be associated with febrile illness, antibiotics,
nutritional deficiencies, preterm birth

A

• Hypomineralized first molars

18
Q

What is the pattern of eruption for primary teeth generally?

A

ABDCE

19
Q

• Mineralization begins at the ___ month of fetal

development

A

4th month (2nd trimester)

20
Q

• Epstein’s pearls –palatal
midline
• Self-limiting without
intervention

A

Inclusion cysts

21
Q
Buccal and lingual 
aspect of alveolus
Most likely ectopic 
mucous glands
No tx indicated
A

Bohn’s Nodules

22
Q
  • Crest of the alveolus

* Remnants of dental lamina

A

Dental Lamina Cysts

23
Q
• Natal at birth/neonatal within 
first 30 days
• Most are actual primary tooth
• May be associated with 
syndrome
• May need to extract if 
aspiration risk or malformed
A

Natal/Neonatal

teeth

24
Q

• Traumatic ulceration
from feeding
• May need to treat
alleviate discomfort

A

Traumatic ulceration: Riga Fede disease

25
Q
• Bluish Swelling
• Asymptomatic
• Treatment is indicated 
when eating is impaired, 
or pain is present
• Cam be associated with 
primary or permanent 
teeth
• Take a radiograph to 
verify tooth position
A

Eruption Hematoma

26
Q
• Evaluate marginal ridges 
in the mouth and on the 
radiograph
• May need to intervene and 
remove the tooth
• Monitor with primary 1st
molars
• Be sure there is a successor
A

Ankylosed or submerged teeth

27
Q

Occurs when a tooth erupts outside of the typical path of eruption

A

Ectopic eruption

28
Q
• Somewhat 
controversial among 
practitioners
• Other professionals 
perform these 
procedures – ENT, 
Plastic surgeons, 
Pediatricians
• If low tethered frenum 
impacts nutrition and 
feeding and/or speech, 
surgical intervention 
may be needed
A

Frenectomy

29
Q

Eruption of the permanent ______ will usually close
the remaining spaces including a midline diastema
if less than approximately 1 mm.

A

canines