Developmental Dental Anomalies II Flashcards

1
Q

What is gemination?

A
  • Attempt of a single tooth bud to divide, resulting in a bifid crown
  • Affects deciduous and permanent dentition
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2
Q

What are the clinical/radiographic features of gemination?

A
  • Tooth count is normal when anomalous tooth is counted as one
  • MC in the anterior maxilla
  • RG: Bifid crown with shared root canal
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3
Q

What does this show?

A

gemination

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4
Q

What is fusion?

A
  • Union of two normally separate tooth buds → form a joined tooth
  • Affects deciduous and permanent dentition
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5
Q

What are the clinical and radiographic features of fusion?

A
  • Tooth count reveals missing tooth when anomalous tooth is counted as one
  • MC in anterior mandible
  • RG: Separate canals usually present
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6
Q

What does this show?

A

fusion

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7
Q

Fusion or gemination?

A

fusion

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8
Q

Fusion or gemination?

A

gemination

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9
Q

What is concrescence?

A

Two fully formed teeth joined by root surfaces by cementum

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10
Q

What are the clinical features of concrescence?

A
  • MC in posterior maxilla
  • Often involves 2nd molar – root in close proximity to 3rd molar
  • May result from postinflammatory/carious tooth
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11
Q

What are the clinical features of a talon cusp?

A
  • Well-delineated additional cusp located on the surface of an anterior tooth
  • Extends at least half the distance between CEJ and incisal edge
  • MC in permanent dentition
  • MC in maxillary lateral > central incisor
  • MC in Asian, Inuit, Native Americans
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12
Q

What does this show?

A

talon cusp

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13
Q

What are the clinical features of dens evaginatus?

A
  • Cusp-like elevation of enamel
  • central groove or lingual ridge of the buccal cusp
  • Observed in posterior teeth (premolar MC)
  • MC in mandible
  • MC in Asian, Inuit, Native Americans
  • May result in occlusal interferences
  • Frequent association with shovel-shaped incisors
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14
Q

What does this show?

A

dens evaginatus

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15
Q

What are the clinincal features of dens invaginatus (dens in dente)?

A
  • Deep surface invagination of the crown or root lined by enamel
  • MC permanent maxillary lateral and central incisors
  • “tooth within a tooth”
  • Opening may become carious
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16
Q

What does this show?

A

dens invaginatus (dens in dente)

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17
Q

What are the clinical features of an enamel pearl?

A
  • Presence of enamel in an unusual location
  • MC max molars > mandibular molars
  • MC at furcation area or near CEJ
  • Precludes normal periodontal attachment
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18
Q

What does this show?

A

enamel pearl

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19
Q

What is taurodontism?

A
  • Enlargement of the body and pulp chamber of a multi-rooted tooth
  • Isolated or syndromic
  • may be associated with cleft lip/palate
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20
Q

What are the clinical features of taurodontism?

A
  • Pulp chambers – increased apico-occlusal height
  • Mild to severe cases
  • MC in permanent teeth
  • May appear bilateral
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21
Q

What does this show?

A

taurodontism

22
Q

What is hypercementosis?

A
  • Non-neoplastic deposition of excessive cementum along the root
  • Isolated or involve multiple teeth
  • Generalized pattern: consider Paget disease
  • Associated with local factors like trauma, inflammation
23
Q

What are the clinical/radiographic features of hypercementosis?

A
  • Thickening or blunting of the root surface
  • MC in mandibular molars
  • Frequency increases with age
24
Q

What does this show?

A

hypercementosis

25
Q

What is a dilaceration?

A
  • Abnormal angulation or bend in the root
  • Majority arise following injury that displaces the calcified portion of the tooth germ
  • Idiopathic or syndromic
26
Q

What are the clinical features of dilaceration?

A
  • MC mand 3rd molars > max 2nd premolar > mand 2nd molar
  • Bend occurs anywhere along the root
  • Complications in extractions or endo
27
Q

What are the different types of developmental alterations of structure?

A
  • Amelogenesis imperfecta
  • Dentinogenesis imperfecta
  • Dentin dysplasia
  • Regional odontodysplasia
28
Q

What is amelogenesis imperfecta?

A
  • A large group of hereditary conditions that show alterations in the enamel in the absence of systemic disease
  • More than 14 different subtypes
  • AD, AR, X-linked inheritance
  • Affects deciduous and permanent dentition
29
Q

In amelogenesis imperfecta, alterations in the enamel may arise at any of the following stages:

A
  • Matrix formation: Hypoplastic
  • Mineralization of matrix: hypocalcified
  • Maturation of the enamel: hypomaturation
30
Q

What are the clinical features of amelogenesis imperfecta?

A
  • Hypoplastic type: may see pits, rows of missing enamel
  • Hypocalcified type: enamel is soft, “cheesy”, easily lost
    — Yellow, brown, orange
  • Hypomaturation type: enamel is soft
    — Opaque white, brown
31
Q

What disorder is this?

A

amelogenesis imperfecta

32
Q

What disorder is this?

A

amelogenesis imperfecta

33
Q

What is dentinogenesis imperfecta?

A
  • Hereditary disturbance in the formation of dentin in the absence of any systemic disorder
  • DSPP gene mutation
  • AD inheritance
  • Affects deciduous and permanent dentition
34
Q

What are the clinical features of dentinogenesis imperfecta?

A
  • Deciduous teeth affected more severely
  • Permanent teeth: MC in incisors and 1st molars
  • MC in White patients
  • Blue to brown discoloration, distinct translucence
  • Enamel strips from poorly formed dentin
35
Q

What are the radiographic features of dentinogenesis imperfecta?

A
  • Bulbous crowns, cervical constriction, thin roots
  • Early obliteration of root canal and pulp chamber

OR
- Normal to enlarged pulp chambers
— Significantly enlarged pulp – “shell teeth”

36
Q

What disorder is this?

A

dentinogenesis imperfecta

37
Q

What disorder is this?

A

dentinogenesis imperfecta

38
Q

What is dentin dysplasia I?

A
  • Loss of organization of root dentin leads to shortened root length
  • AD inheritance
  • Type II thought to be a variant of dentinogenesis imperfecta
  • Deciduous and permanent teeth affected
39
Q

What are the clinical features of dentin dysplasia I?

A
  • Enamel and coronal dentin well-formed
  • Radicular dentin loses organization → short roots
  • Tooth mobility and premature exfoliation
40
Q

What are the radiographic features of dentin dysplasia I?

A
  • Deciduous teeth: little or no detectable pulp, very short roots
  • Permanent teeth: crescent shaped pulpal remnant, short roots
41
Q

What disorder is this?

A

dentin dysplasia I

42
Q

What is regional odontodysplasia?

A
  • Nonhereditary developmental abnormality of teeth that affects enamel, dentin, and pulp
  • Most cases are idiopathic, some syndromic
  • May be due to alteration of vascular supply
43
Q

What are the clinical findings for regional odontodysplasia?

A
  • Enamel, dentin, and pulp affected
  • MC maxillary anterior teeth
  • Dx at time of eruption of primary and permanent
  • Affects several teeth, quadrant distribution
  • Impacted teeth, delayed eruption
  • Erupted teeth are malformed, caries rampant
  • Hyperplasia of overlying soft tissue
44
Q

What are the radiographic findings for regional odontodysplasia?

A
  • Extremely thin enamel and dentin
  • Enlarged pulp chambers – ghost teeth
  • Short roots may be observed
45
Q

What disorder is this?

A

regional odontodysplasia

46
Q

What is segmental odontomaxillary dysplasia?

A

Developmental disorder, affects jaw and overlying soft tissue

47
Q

What are the clinical features of segmental odontomaxillary dysplasia?

A
  • Painless, unilateral enlargement of maxillary bone
  • Usually dx during childhood
  • Hyperplasia of overlying gingiva
  • Primary teeth may be hypoplastic
  • Maxillary premolar teeth may be missing
48
Q

What are the radiographic features of segmental odontomaxillary dysplasia?

A
  • Thickened trabeculae, often vertically oriented
  • Radiopaque, granular appearance
  • Maxillary sinus may be smaller
49
Q

What is the treatment for segmental odontomaxillary dysplasia?

A
  • Remains relatively stable, may not require tx
  • Surgical recontouring
50
Q

What disorder is this?

A

Segmental odontomaxillary dysplasia