Abnormalities of tooth number, tooth size, tooth shape Flashcards

1
Q

Tooth development - revise

A

Tooth development - revise

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2
Q

Tooth development in stages (3)

A

• Initiation
starts tooth formation and ensures the right number of
teeth in the correct location in the jaws
• Morphodifferentiation
formation of teeth of the correct shape
• Cytodifferentiation
differentiation of cells to produce specific dental tissues

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3
Q

Tooth development phases (2)

A
  1. crown formed first

2. then root formation

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4
Q

Aetiology of dental anomalies (2)

A

Genetic

Environmental

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5
Q

Environmental factors - Localised (2)

A

Trauma

Infection

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6
Q

Environmental factors - generalised (2)

A

Infection

Drugs

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7
Q

Aetiology of dental anomalies - multifactorial determination (2)

A

Genetic component - polygenic

Environmental component

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8
Q

Occasional major influences on dental anomalies (4)

A

• Chromosomal anomalies e.g. Down syndrome
(Chromosomal gain, loss)
• Single gene syndromes e.g. Ectodermal dysplasia
• Single genes of localised effect e.g. maxillary lateral incisors
• Environmental insults e.g. rubella, thalidomide, irradiation

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9
Q

Cellular response to stimuli (4)

A
  1. Developmental stage
  2. Adaptive range
  3. Stimulus severity, duration, interaction
  4. Individual’s response capacity
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10
Q

Anomalies involving tooth number (3)

A
  1. Hypodontia (oligodontia, -6)
  2. Supernumerary teeth (hyperdontia)
  3. Anodontia
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11
Q

Primary hypodontia stats (4)

A

B most common
Max > mand
F = M
0.1-0.9% Caucasian

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12
Q

Secondary hypodontia stats (6)

A
8 most common (practical)
max = mand
8 > 5 > upper 2 > 4 (Europeans)
F : M 4 : 1
3.5 - 6.5% (9-37%)
mild, moderate, severe (oligo)
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13
Q

Aetiology of hypodontia (5)

A
• Obscure
• Polygenic, plus intrauterine systemic factor
• Increased frequency of 
-low birth weight
-multiple births
-increased maternal age
• Single gene mainly for 2
• PAX9, MSX1
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14
Q

Hypodontia occurs with (3)

A

Down Syndrome
Rubella, thalidomide embryopathy
Cleft lip/ palate

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15
Q

Severe hypodontia and microdontia occur with (2)

A

X-linked hypohidrotic ectodermal dysplasia
AR chondroectodermal dysplasia
(Ellis–van–Creveld Syndrome) i.e. syndromes

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16
Q

Supernumerary teeth types (3)

A

Supplemental - normal series
Accessory - atypical form
Location - e.g. Mesiodens
adjacent to midline suture

17
Q

Most common regions of supernumararies (3)

A

Premaxilla - most common region
75% not erupt - chance finding
May prevent eruption - e.g. mesiodens

18
Q

Epidemiology of supernumeraries (4)

A
• 1° - 0.2 - 0.8%
• 2° - 1.5 - 3.5% unilateral
M : F 2:1
• maxilla : mandible 5:1
• 30-50% of primary in premaxilla followed by permanent
19
Q

Associations with supernumerary teeth (3)

A
• Invaginated teeth
• Palatal clefts
• Syndromes
-cleidocranial dysplasia
-oral-facial-digital syndrome
-Gardner syndrome
20
Q

Tooth size anomalies (2)

A
  1. Microdont

2. Megadont/macrodont ( upper 1, 5 )

21
Q

Microdontia stats (4)

A
  • 1° - uncommon (0.2 - 0.5%)
  • 2° - 2.5%
  • F > M
  • Unusual form, tapering
22
Q

Megadontia / macrodontia (3)

A
• 1.1% permanent dentition
• Generalised
-pituitary gigantism
-unilateral facial hyperplasia
• Isolated megadont -hereditary gingival hyperplasia
-hypertrichosis
23
Q

Aetiology of megadontia (3)

A

• Multi-factorial - polygenic + environment
-for microdontia
• Single gene inheritance described
• Associated with Down, Ectodermal dysplasia

24
Q

Tooth form - double teeth - what can go wrong (5)

A
  • fusion, gemination…
  • labial segment mand > max (1°)
  • incisors frequent (2°)
  • 1° > 2° (0.5 - 1.6%)
  • F = M
25
Q

Tooth form - double teeth - why? (5)

A
  • Mode of development unclear
  • ?Genetic
  • Minor notch to almost separate crowns
  • plus/ minus common pulp space, root canal
  • Concrescences
26
Q

Accessory cusps that exist (3)

A

• Carabelli (6s)
• Talon (1s + 2s)
• Buccal cusp (paramolar tubercles)
(4s + 5s and molars)

27
Q

Double teeth - what are the implications (2)

A

• Permanent anomalies follow double primary teeth
-30 - 50% Caucasian
-70% Japanese
• Delayed eruption due to retarded root resorption

28
Q

Invaginated tooth (odontome) stats (4)

A
• Permanent (1 - 5%), maxillary incisors
• enamel epithelium into dental papilla
• dens in dente, invaginated odontome
• deep cingulum pit ........
• M : F 2 : 1
• Bilateral symmetry (plus supernumeraries)
• Enamel complete
incomplete
• Dentine missing
29
Q

Evaginated tooth (odontome ) stats (4)

A
• Premolars
• Enamel epithelium or focal hyperplasia of
ectomesenchyme
• Rare in Caucasians
• Enamel, dentine, pulp
30
Q

Root size (4)

A
1. Large - 3’s
M > F (5 : 1)
2. Small - 1., 2.
dentine dysplasias
• Irradiation - shortened roots
• Racial variation
31
Q

Root form anomalies - taurodontism (4)

A

Multi-rooted
Crown elongated corono-apically
ACJ constriction (cervix) absent
Syndromes + polygenic inheritance

32
Q

Root form anomalies - accessory roots (4)

A

Carabelli tubercle
Paramolar tubercle
Enamel pearls
Trauma or genetic

33
Q

Root form anomalies - pyramidal roots (1)

A

Multi-rooted (fused)

34
Q

Root form anomalies

A

Taurodontism
Accessory roots
Pyramidal roots