Developmental anomalies in orthodontics Flashcards

1
Q

What are supernumerary teeth?

A

A tooth (or tooth like structure) that is additional to the normal series

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2
Q

What is the incidence of supernumeraries?

A

Low, 35% of cases in the primary dentition are superseded by supernumerary in the permanent. They are 2x as common in males and 5x more common in the maxilla than mandible.

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3
Q

How do we classify supernumeraries?

A

Supplemental - extra tooth of normal ish form
Conical - generally early forming and peg shaped
Tuberculate - generally late forming and barrel shaped

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4
Q

What is an odontome and how are they classified?

A

A mass of dental structures
Compound - containing many small separate tooth like structures (denticles) - usually found anteriorly
Complex - a large mass of disorganised enamel and dentine - usually found posteriorly

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5
Q

Classification by site of supernumeraries?

A

Mesiodens - midline between the central incisors
Paramolar/parapremolar - adjacent to the molars/premolars
Distodens/distomolar - distal to the arch

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6
Q

What are conical supernumeraries?

A

Peg shaped
Mesiodens if on the midline - can cause diastema
Root formation ahead or with permanent incisor
Unlikely to impede eruption or may itself erupt
If high and will not interfere with orthodontic treatment, it can be left
If on the palate it can be removed under LA as it can be difficult to clean
Risk of cystic change or resorption low

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7
Q

What are tuberculate supernumeraries?

A

Barrel shaped
Root formation is delayed compared to permanent incisor
Usually palatal
More likely to impede eruption
Often occur in pairs
Usually need to be removed - usually surgical

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8
Q

What are the associated conditions with supernumeraries?

A
  • cleft lip and palate
  • gardner’s syndrome - causes multiple polyps in the colon and osteomas - tumours in the skull
  • cleidocranial dysostosis - inherited/new mutation gene, collarbones completely/partly missing and hyperplastic maxilla
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9
Q

What are the problems with supernumeraries?

A
  • impede eruption of other teeth
  • cause displacement or rotation of erupted teeth
  • produce spacing between erupted teeth
  • contribute to crowding if they erupt
  • undergo cystic change
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10
Q

What is hypodontia?

A

The developmental absence of one or more teeth <6

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11
Q

What is the most common tooth to be missing in hypodontia?

A

L5’s > U2’s > U5’s > L1’s

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12
Q

Is hypodontia more common in women or men?

A

Women 3:2

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13
Q

What is oligodontia?

A

Absence of >6 teeth

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14
Q

What is anodontia?

A

Absence of all teeth

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15
Q

What are the associated conditions with hypodontia?

A

Cleft lip and palate
Downs syndrome
Ectodermal dysplasia - defects of hair, skin, nails, sweatglands

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16
Q

What is the treatment options for hypodontia?

A

Open the gap with orthodontics and replace with bridge, denture, implant or close the gap and camouflage teeth

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17
Q

What is microdontia?

A

Teeth which have smaller than average dimensions - range from mildly to severely microdont
Can affect the crown, root or whole tooth
Upper 2’s are mostly affected - peg shaped laterals - can often see this in one upper 2 and then the other lateral incisor missing

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18
Q

What are the treatment options for microdontia?

A

Accept - generally done if mild or in a less aesthetically pleasing area
Create space to have the microdont teeth built up - composite, veneer, 3/4 crown
Extract the microdont tooth and close the space and adjusting canine to look like a lateral

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19
Q

What is macrodontia/megadontia?

A

Teeth which have larger than average dimensions
Can affect the crown, the root or the whole tooth
Upper 1’s/lower 5’s are most commonly affected - often bilateral
Often but not always can be differentiated from a double tooth by lack of coronal notching and normal pulpal form

20
Q

What are treatment options for macrodontia?

A

Accept - generally done if mild or in a less aesthetically challenging area (lower 5’s)
Extract and reduce space for a normally sized prosthesis
Extract and close space
Camouflage restoratively to resemble 2 teeth (If a very large upper 1 and missing upper 2) eg crown

21
Q

What are double teeth?

A

Fusion of 2 separate tooth germs leading to a reduced number of teeth in the arch
Gemination - developmental separation of a single tooth germ
More common in primary (0.5-1.6%) than secondary (0.1-0.2%) dentition and anteriorly rather than posteriorly
Clinically varies from a small notch on a wide crown/root to 2 apparently separate crowns with a shared root
Concrescence - fusion of the roots only (freq terminal molars)

22
Q

What are the treatment options for double teeth?

A

Generally no intervention needed in the primary dentition
Be wary of caries at the interface between the 2 crown segments, especially if extending subgingival - may want to restore any notch for aesthetic and preventative reasons - flowable composite
If 2 separate root canals - can surgically divide - specialist
Extraction - if caries into the pulp, replacement and closure of space depending on malocclusion

23
Q

What is invagination?

A

An enamel lined ‘infolding’ in the crown of a tooth, which can extend into the root
Produced by an invagination of the enamel epithelium into the dental papilla during development
Upper 2’s most commonly affected, followed by upper 1’s
Milder forms appear similar to a deep cingulum pit (Dens invaginatus)
In more severe forms the invagination starts at the incisal edge (dens in dente) and can lead to a grossly abnormal crown and root

24
Q

What is the management of invagination?

A

Although defects are generally enamel lined it can be quite poor and thin
Difficulty cleaning means high caries risk and bacterial ingress to the pulp leading to pulpal disease
Can try to maintain less severe forms with adhesive restorations (fissure sealants, small composites) - early intervention is key
Can attempt RCT but often challenging due to abnormal morphology
If grossly abnormal, extraction may be best with closure of prosthetic replacement

25
Q

What are accessory cusps?

A

Additional outward projections of enamel and dentine off the body of the tooth proper.
Fairly common - cusp of Carabelli
Talon cusp - on maxillary incisors - check for caries at the interface
Size and pulpal involvement varies
If causing occlusal interferences - may need to be reduced - if extensive reduction may require a pulpotomy (take PA)

26
Q

What is a dilaceration?

A

An abrupt deviation along the long axis of the crown or root
Upper incisors most commonly affected, can lead to failure of eruption
Management: if less marked divergence, can expose, bond traction and attempt orthodontic alignment - need to consider where the root will end up once the crown is aligned (if at right angle to crown may end up coming through labial sulcus)
If more significant will likely need to remove - extraction can be challenging.

27
Q

What are the causes of dilaceration?

A

Traumatic - due to intrusion of primary incisor into developing tooth germ
Position of dilaceration corresponds with stage of development at time of trauma
Generally crown angled palatally and hypoplasia at the site of dilaceration

Developmental - may be due to an obstruction of the eruption path
- generally crown angled upward and labially and no hypoplasia is seen
Upper 1’s most affected

28
Q

What is delayed eruption and when do we investigate?

A

When a tooth has not erupted in line with normal timings, if a tooth hasn’t erupted 6 months after its contralateral, investigate
Localised delays often do require intervention

29
Q

What are causes of delayed eruption?

A

Cleidocranial dysplasia, down syndrome, cleft lip and palate, hereditary gingival hyperplasia
Crowding, supernumeraries, trauma, ectopic tooth germ, early loss of primary teeth, retention of primary teeth, local pathology and transpositions

30
Q

What are ectopic teeth?

A

teeth in an abnormal place or position

31
Q

What are impacted teeth?

A

Physical impediment to eruption by another structure sucj as bone, adjacent teeth and soft tissues.

32
Q

Which directions will impacted teeth come out?

A

Upper - palatal
Lower - lingual

33
Q

What are the causes of unerupted upper canines?

A

Genetic - family history, > frequency bilateral than expected, associated malformations
Guidance theory - missing or absent lateral incisor, retention of primary canine and crowding

34
Q

What are the consequences of unerupted upper canines?

A

Root resorption - up to 2/3rds of U2’s have root resorption when U3’s are ectopic
Most root resorption occurs before 14

Coronal resorption - most likely in adults
Cystic change - generally thought to be low risk

35
Q

When do we screen for maxillary canines?

A

Majority of the normal erupting canines should be palpable in the buccal sulcus by 10 years old, start palpating at 9.
If you cannot palpate by 10 consider referral

36
Q

When are eruptions of canines considered late?

A

12.3 - girls
13.1 - boys

37
Q

What is a mechanical failure of eruption (ankylosis)?

A

Uncommon isolated condition causing a localised failure of eruption of a single tooth with no other identifiable causes.
Other teeth are apparently normal, may appear to submerge due to the vertical growth of the alveolar complex and other teeth surrounding - tooth gets fused into bone and is infraoccluded. Teeth fail to respond to orthodontic forces.

38
Q

What is primary failure of eruption?

A

Rare isolated condition causing localised failure of eruption of multiple teeth with no other identifiable causes.
- Primarily affects posterior teeth
- Affects all teeth posterior to the most anteriorly affected tooth leading to a lateral open bite and the teeth fail to respond to orthodontic forces so require restorative options to manage

39
Q

What is cleft lip and palate?

A

Congenital disorder affecting the lip and palate affecting males more than females

40
Q

What is cleft palate?

A

An isolated congenital condition affecting just the palate and affecting females more than males

41
Q

What syndromes are associated with CLP?

A

Treacher collins, van der Woude, hypohydrotic ectodermal dysplasia and Down syndrome.

42
Q

What is a characteristic of Van der Woude?

A

A pitting of the lower lip

43
Q

What is Down Syndrome?

A

Trisomy of chromosome 21

44
Q

What are the key dental findings of patients with Down Syndrome?

A

Class III malocclusion - maxillary hypoplasia
Hypodontia
CLP
Microdontia
Delayed eruption of secondary dentition
Short roots

45
Q

Hypohydrotic ectodermal dysplasia

A

Smooth dry skin with sparse hair with total or partial absence of sweat glands.

46
Q

What are the dental findings of hypohydrotic ectodermal dysplasia?

A

Class III malocclusion
Anodontia/severe hypodontia
Deformed teeth/conical crowns
Delayed eruption
Xerostomia
CLP