Anomalies Flashcards

1
Q

Turner’s Hypoplasia (Enamel)

A
  • Periapical inflammatory disease of overlying deciduous tooth
  • Varies from focal areas of white to yellow to brown discoloration to extensive hypoplasia
  • Permanent PM frequent
  • Anterior teeth less frequent bc crown formed before development of PA disease
  • Cause: Trauma or caries in deciduous teeth
  • MX CIs common
  • Clinical appearance of permanent successor dependent on timing and severity of damage
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2
Q

Hypoplasia from Exanthematous Fever

A
  • Age 2-3: Rows of pits or diminished enamel on permanent anterior incisors & M1s
  • Age 4-5: Similar pattern seen in cuspids, bicuspids, M2s
  • Temporal line: Line of deformed enamel
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3
Q

Fluorosis

A
  • Fluoride enamel defects through retention of amelogenin proteins in enamel
  • Creates hypomaturation of enamel, alters light reflection and gives white chalky areas
  • Critical period is 2nd to 3rd yr of life when permanent teeth are forming
  • Dose dependent from 1.2ppm to 0.7ppm w/ fluorosis in excess of 2.0ppm
  • Local excess fluoride from toothpaste ingestion or from fluoride supplements given to infant
  • Long term excess fluoride in H2O
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4
Q

Congenital Syphilis

A
  • Transmitted across placenta from infected mother to fetus
  • In untreated mother
  • Oral Manifestations
    • Hutchinson’s Incisors: Anterior teeth have crowns shaped like flat screwdrivers
    • Mulberry Molars: Posterior teeth have constricted occlusal tables w/ disorganized surface anatomy
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5
Q

Tooth wear

A
  • Normal physiologic loss of dental structures
    • Considered pathologic when creates functional, esthetic, or dental sensitivity
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6
Q

Attrition

A

Loss of tooth structure caused by tooth to tooth contact

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7
Q

Abrasion

A

Pathologic wearing of tooth structure by mechanical action of external agent

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8
Q

Erosion

A

Loss of tooth structure caused by nonbacterial chemical process

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9
Q

Perimolysis

A

Erosion from dental exposure to gastric secretions

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10
Q

Abfraction

A
  • Loss of tooth structure from occlusal stresses that create tooth flexure w/ failure of enamel and dentin
    • Enamel rods are weaker under compression than tension
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11
Q

Ankylosis

A
  • Anatomic fusion of cementum or dentin to bone
  • Cause unknown
  • Teeth frequently involved
    • Primary MN M1
    • Primary MN M2
    • Primary MX M1
    • Primary MX M2
  • Rarely permanent teeth
  • Tx
    • Ortho cannot move teeth
    • Extraction of tooth will allow permanent tooth to erupt
    • No permanent tooth: Esthetic build up
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12
Q

Hypodontia

A
  • Denotes lack of one or more teeth
  • Anodontia: Complete lack of tooth development
    • Anodontia is rare and associated w/ ectodermal dysplasia
  • Oligodontia: Lack of 6 or more teeth
  • Absence of missing primary = strong chance of missing permanent successor
  • M3s, MN PM2, MX LIs
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13
Q

Anodontia

A
  • Complete lack of tooth development
  • Rare and associated w/ ectodermal dysplasia
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14
Q

Oligodontia

A

Lack of 6 or more teeth

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15
Q

Hyperdontia

A
  • Development of increased # of teeth
  • Supernumerary tooth: Single tooth hyperdontia
    • 75% of cases
    • 95% in MX
  • Most common in incisor region
  • Mesiodens: Supernumerary tooth in MX incisor area
  • Distomolar: Supernumerary M4
  • Paramolar: Supernumerary buccal or lingual to molar tooth
  • Natal or Neonatal teeth: 85% are primary MN incisors
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16
Q

Supernumerary tooth

A
  • Single tooth hyperdontia
  • Most common in incisor region
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17
Q

Mesiodens

A

Supernumerary tooth in MX incisor area

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18
Q

Distomolar

A

Supernumerary M4

19
Q

Paramolar

A

Supernumerary buccal or lingual to molar tooth

20
Q

Natal or Neonatal Teeth

A

85% are primary MN incisors

21
Q

Microdontia

A
  • Unusually small teeth
  • Peg lateral (MX lats) are most frequent, followed by M3
22
Q

Macrodontia

A

Larger than avg teeth

23
Q

Gemination

A

Single enlarged tooth or joined (double) tooth in which the tooth count is normal, when anomalous tooth is counted as one

24
Q

Fusion

A

Single enlarged tooth or joined (double) tooth in which the tooth count is missing a tooth, when anomalous tooth is counted as one

25
Q

Concresence

A

Union of 2 teeth by cementum alone w/o confluence of underlying dentin

26
Q

Dilaceration

A

Bend in tooth root

27
Q

Cusp of Carabelli

A

Accessory cusp located on palatal surface of ML cusp of MX molar

28
Q

Talon Cusp

A

Well-delineated additional cusp located on the surface of anterior tooth and extends half the distance from CEJ to incisal edge

29
Q

Dens Evaginatus

A
  • Cusp-like elevation of enamel
  • Located in central groove or lingual ridge of buccal cusp of PM or M teeth
  • Usually located
    • MN teeth
    • PM teeth
    • Bilateral
  • Tx
    • No occlusal interference: No tx
    • Occlusal interference: Elimination of opposing occlusal interference
30
Q

Dens Invaginatus

A
  • Deep surface invagination of crown or root that is lined by enamel
  • Two types
    • Coronal Dens Invaginatus
      • More common
      • Dens in dente: Invagination resembles tooth w/in a tooth
      • Dilated odontome: Invagination dilates and disturbs root/tooth formation
    • Radicular Dens Invaginatus
  • Tx
    • Small invaginations: Restoration after eruption
    • Larger invaginations: Endo tx or extraction
31
Q

What type of dens invaginatus is most common? Coronal or radicular?

A

Coronal dens invaginatus

32
Q

Dens in dente

A

Coronal dens invaginatus

Tooth w/in a tooth

33
Q

Dilated odontome

A

Coronal dens invaginatus

Invagination dilates and disturbs root/tooth formation

34
Q

Taurodontism

A
  • Enlargement of body and pulp chamber of a multi-rooted tooth w/ apical placement of pulpal floor and bifurcation of roots
  • Tx: None required
35
Q

Hypercementosis

A
  • Cemental hyperplasia
  • Non-neoplastic deposition of excessive cementum
  • Continuous w/ normal radicular cementum
  • Enlarged root
  • Surrounded by RL PDL space
  • Lamina dura intact
36
Q

Amelogenesis Imperfecta

A
  • 14 different hereditary subtypes of developmental alterations of enamel in the absence of systemic disease
  • Different classification schemes
    • Wiktop’s classification: Phenotype & pedigree
      • Hypoplastic
      • Hypomaturation
      • Hypocalcified
      • Gene mutations
  1. Hypoplastic AI
  2. Hypermaturation AI
  3. Hypocalcified AI
  4. AI w/ Taurodontism
37
Q

Hypoplastic AI

A
  • Inadequate deposition of enamel matrix
  • Any matrix present is mineralized
  • Generalized pattern: Pin-point pits scattered across surface of the teeth
  • Localized pattern: Horizontal rows of pits
  • AD smooth pattern
  • X-linked smooth pattern
38
Q

Hypomaturation AI

A
  • Enamel matrix laid down properly and begins to mineralize
  • Defect in maturation of enamel
  • Normal shape, discolored, enamel chips off
  • Pigment pattern: Mottle brown color; punctured by explorer
  • X-linked pattern: Enamel chips, pierced by explorer
  • Snow-capped pattern: White opaque enamel on incisal or occlusal third of crown
39
Q

Hypocalcified AI

A
  • Enamel matrix laid down properly
  • No mineralization occurs
  • Enamel very soft and easily lost
40
Q

Dentinogenesis Imperfecta

A
  • Hereditary development disturbance of the dentin in the absence of systemic disorder
  • Mutation of DSPP gene
  • 8 different mutations
  • Clinical & Rad Features
    • Translucent teeth
    • Blue to brown discoloration
    • Bulbous crowns, cervical constriction
    • Thin roots
    • Obliteration of root canals and pulp chamber
  • Dentinogenesis Imperfecta vs. Osteogenesis Imperfecta w/ Opalescent Teeth
    • OI: AD Type 1 Collagen disorder; COL1A1, COLA12 gene mutation
    • DI: DSPP gene mutation
      • 8th mutation DSPP is known to cause dentin dysplasia Type II (more closely related to dentinogenesis imperfecta)
41
Q

Dentin Dysplasia

A
  • Developmental defect of dentin
  • Loss of dentin organization
  • No evidence of systemic disease or DI
  • Two types
    • Type I: Radicular Dentin Dysplasia
    • Type II: Coronal Dentin Dysplasia
42
Q

Type I Dentin Dysplasia

A

Type I: Radicular Dentin Dysplasia

  • Rootless teeth
  • Tooth mobility & premature exfoliation
  • Pulpal obliteration
  • Rarefying osteitis w/o cause
43
Q

Type II Dentin Dysplasia

A

Type II: Coronal Dentin Dysplasia

  • Caused by DSPP mutation
  • Root length normal
  • Pulp chambers enlarged
    • Thistle-tube-shaped or flame shaped