Developmental anomalies in orthodontics Flashcards

1
Q

define supernumeraries ?

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
  • 2-4% permanent dentition, 0.8% primary dentition (Caucasians)
  • 35-50% of cases in the primary dentition superseded by
    supernumerary in the permanent dentition
  • In the permanent dentition = twice as common in males and maxilla 5 times more common than mandible
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3
Q

how do we classify supernumeraries ?

A

by form or site

  1. FORM
    * Supplemental – extra tooth of normal (ish) form
    * Conical – generally early forming and peg shaped
    * Tuberculate – generally late forming and barrel shaped
    * Odontome ( 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
  2. SITE
    * Mesiodens – midline between the central incisors
    * Paramolar / parapremolar – adjacent to the molars / premolars
    * Distodens/Distomolar – distal to the arch
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4
Q

what is the most common supernumerary ?

A

conical

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5
Q

where are conicals usually found ?

A

midline so mesiodens - can cause diastema

  • can erupt in palate
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6
Q

when do conicals form?

A
  • root formation is usually ahead or with the permanent incisors
  • unlikely to cause problems ie. impede eruption and may itself erupt
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7
Q

how do we manage conicals ?

A

if high and will not interfere with ortho tx = can be left
- the risk of cystic change or resorption is low

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8
Q

tuberculate: describe them? when are they formed ? when do they erupt? management ?

A
  • Barrel shaped
  • Root formation delayed compared to
    permanent incisor
  • Usually palatal
  • More likely to impede eruption
  • Often occur in pairs
  • Usually need to be removed
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9
Q

what are some associated conditions with supernumeraries ?

A
  • Cleft lip and palate
  • Gardner’s syndrome
  • Cleidocranial dysostosis
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10
Q

what are some of the problems associates with supernumeraries ?

A

In the permanent dentition, the majority fail to erupt and are incidental radiographic findings.
However, they can:
* 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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11
Q

what can cystic change cause ?

A

swelling
resorption of roots
displacement of teeth
discomfort

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12
Q

what is hypodontia? prevalence ?

A
  • The developmental absence of one or more teeth
    (excluding 8s – 25% to 35% absent)
  • Prevalence of 6.4% (varies amongst populations)
  • L5s (2.6%) > U2s (2%) > U5s > L 1s
  • Genetic aetiology - MSX1, PAX9 and AXIN2
  • Females 3:2
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13
Q

how can we classify hypodontia?

A
  • Mild (1-2), moderate (3-5) and severe (>6)
  • or
  • Hypodontia – absence of <6
  • Oligodontia –absence of ≥6 teeth
  • Anodontia – absence of all teeth
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14
Q

what are some associated conditions of hypodontia ?

A
  • Cleft lip and palate
  • Downs syndrome
  • Ectodermal dysplasia
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15
Q

How do we treat hypodontia ?

A
  • open space and replace missing teeth with prosthetics
  • orthodontics and camouflage teeth
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16
Q

what is microdontia? prevalence ?

A
  • Teeth which have smaller than average dimensions – range from
    mildl to severe
  • Can affect the crown, the root or the whole tooth
  • Most likely genetic aetiology
  • Around 2.5% of people have at least one microdont tooth
  • Can affect just one tooth, many teeth or even the entire dentition
    (although this is rare and generally associated with an underlying
    syndrome)
  • Upper 2s are most commonly affected – ‘peg’ laterals
  • Often see one peg upper 2 and one missing upper 2
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17
Q

tx option for microdontia?

A
  • Accept – generally done if mild or in a less aesthetically
    challenging area e.g. upper 7s
  • Create space to have the microdont teeth built up
  • Extract the microdont tooth and close the space
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18
Q

what is macrodontia ?

A
  • Teeth which have larger than average dimensions
  • Can affect the crown, the root or the whole tooth
  • Most likely genetic aetiology
  • Around 1% of people have at least one megadont tooth
  • Upper 1s / lower 5s 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
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19
Q

tx options for macrodontia?

A
  • Accept – generally done if mild or in a less aesthetically
    challenging area e.g. lower 5s
  • Extract and reduce space for a normally sized prosthesis
  • Extract and close space
  • Camouflage restoratively to resemble 2 teeth e.g. if a very large
    upper 1 and missing upper 2
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20
Q

what is double teeth ? prevalence?

A
  • some cases in macrodontia we can get double teeth. They can be because of fusion or germination.
  • Fusion – of 2 separate tooth germs leading to a reduced number
    of teeth in the arch
  • Gemination – developmental
  • you can investigate from radiographs and clinically 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
  • Males : Female 1 : 1
  • 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 (frequently terminal
    molars)
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21
Q

what is a related condition to double teeth ?

A

concrescence- cementum of 2 adjacent teeth fuses
- this happens usually with 6s or 7s
- can only diagnosed via cbct
can make extractions difficult

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22
Q

tx options fro double teeth?

A
  • no intervention needed in primary dentition
  • Be wary of anomalies in the permanent dentition including: hypodontia and supernumaries (30-50% penetrance)
  • 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
  • If 2 separate root canals – can surgically divide
  • Extraction
23
Q

what is invagination? prevalence ?

A

An enamel lined ‘infolding’ in the crown of a tooth, which can extend
into the root

  • 1 – 5% of people depending on ethnicity and inclusion criteria
  • Produced by an invagination of the enamel epithelium into the dental
    papilla during development
  • Upper 2s most commonly affected, followed by upper 1s
  • Milder forms appear similar to a deep cingulum pit (Dens Invaginatus)
  • In more severe forms the invagination starting at the incisal edge (Dens
    in Dente) and can lead to a grossly abnormal crown and root
24
Q

how do we manage invagination ?

A
  • Although defects are generally enamel lined, this can be of poor
    quality and very 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
  • Early intervention is key!
  • Can attempt RCT but often challenging due to abnormal morphology
  • If grossly abnormal, extraction may be the best option with space
    closure of prosthetic replacement
25
Q

what are accessory cusps ? prevalence ?

A
  • Can affect primary and secondary dentition
  • Fairly common – 10 - 60% of people have a cusp of Carabelli on an
    upper 6 (depending on population studied)
  • ‘Talon cusp’ on maxillary incisors – check for caries at interface
  • Size and pulpal involvement varies
  • If causing occlusal interferences may
    need to be reduced
  • If extensive reduction may require
    a pulpotomy
26
Q

what is dilacertion ?

A
  • An abrupt deviation along the long axis of the crown or root
  • Upper incisors most commonly affected
  • Can lead to failure of eruption
27
Q

what is the management for dilaceration ?

A
  • 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 more significant, will likely need to remove – extraction can be challenging!
28
Q

aetiology of dilacerations (kink) ?

A

TRAUMATIC – due to intrusion of a primary incisor into developing tooth germ
* Position of dilaceration corresponds with stage of development at time of trauma
* Generally crown angled palatally and hypoplasia seen 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 commonly affected

29
Q

when would w investigate delayed eruption further ?

A

there can be great individual variation interruption times in permanent dentition:
* Eruption sequence is therefore most important
* If a tooth still hasn’t erupted > 6/12 after its contralateral, =investigate

Generalised delayed eruption isn’t a cause for concern nor does it require any intervention other than reassurance

Localised delays often do require intervention

30
Q

list some systematic conditions leading to delayed eruption ?

A
31
Q

list some local factors leading to delayed eruption ?

A
32
Q

what are the 2 types of transpositions ?

A

pseuodetranspostion = just crown that are in swapped position

true transposition = whole tooth tooth including the root in wrong position

most common transposition = maxillary lateral incisor - canine transposition

33
Q

what are the 2 types of unerupted teeth ?

A
  • Ectopic – developed in abnormal place or position
  • Impacted – physical impediment to eruption by another structures such as bone, adjacent teeth, soft tissues
34
Q

what sorts of problems arrise around upper 1’s?

A

dilacerations or obstructions

35
Q

what sorts of issues arise with upper and lower 5’s ?

A

lack of space/ obstruction

36
Q

what sorts or issues arise with upper 6s ?

A

impaction into E’s

37
Q

what sorts of issue arise with upper and lower 8’s ?

A

lack of space in arch causing impaction

38
Q

what is the prevalence of unerupted upper canines ?

A

2% maxillary canines (Caucasian)
61% palatal / 34% in line of arch / 4.5% buccal (ectopic)
Female : Male 7 : 3

39
Q

what is the aetiology of unerupted upper canines ?

A

Polygenic and multifactorial
Genetic theory
* Family history
* > frequency bilateral than expected
* Associated malformations

Guidance theory / local factors
* Missing or absent lateral incisor (helps guide canine)
* Retention of 1ry canine
* Crowding

40
Q

what are some of the consequences of unerupted upper canines ?

A

Root resorption
* Up to 2/3 U2s have RR when U3s
ectopic
* Most RR occurs before 14
* How much is clinically significant?
Coronal resorption
* Most likely in adults
Cystic change
* Generally thought to be low risk,
especially in older patients

41
Q

how do we screen for canines ?

A

Majority of normal erupting maxillary canines should be
palpable in the buccal sulcus by 10 years old
CaNINE! – Start palpating at 9
Considered late if not erupted before 12.3 years in girls and
13.1 years in boys
Both U3s should erupt within 6 months of each other
< 0.1% of U3s are developmentally absent
If can’t palpate by 10, consider referral for specialist opinion

42
Q

what is ankylosis (failure of eruption)? why does it happen?

A

Uncommon, isolated condition causing a localised failure of eruption of a single tooth with no other identifiable causes
* No obvious impediment to eruption
* Other teeth apparently normal
* May partially erupt and then appear to submerge due to continued vertical growth of the rest of the alveolar complex
* The teeth fail to respond to orthodontic forces – often removal is indicated
* Localised disturbances in metabolism or trauma often implicated. May have a genetic component.

43
Q

what is primary failure of eruption? consequences ? causes?

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
  • Leads to a lateral open bite
  • The teeth fail to respond to orthodontic forces
  • Generally restorative options required to manage
  • Strong genetic component – PTH1R
44
Q

what are some conditions/ syndromes commonly associated with dental anomalies more commonly seen in ortho?

A
  • cleft lip and palate
  • downs
  • Hypohydrotic Ectodermal Dysplasia
  • Cleidocranial Dysostosis
45
Q

what is cleft lip and palate? prevalence ?

A
  • most common
  • 1 in 700 to 1 in 1000 live births (Caucasians)
  • More common in Asian (1:500) and less common in African
    (1:2500) populations
  • 2 : 1 Males : Females
46
Q

what is cleft palate syndrome?

A
  • 1 in 2000 live births (Caucasians), but less racial variation
  • 4 : 1 Females : Males
  • doesn’t affect lip
47
Q

how much of CP and CLP are syndromic? and what are the syndromes ?

A

Treacher Collins, van der Woude, hypohydrotic ectodermal
dysplasia, Down syndrome

48
Q

label diagram

A

a= unilateral CL
b= bilateral CL
c= unilateral CLP
d= bilateral CLP
e= isolated CP

49
Q

what is downs and what are the key dental findings?

A
  • 1 in 700 live births overall, risk increases with maternal age
  • Trisomy of chromosome 21
  • Myriad signs and symptoms
  • Key dental findings include
  • Class III malocclusion - maxillary hypoplasia
  • Hypodontia
  • CLP
  • Microdontia
  • Delayed eruption of 2ry dentition
  • Short roots
50
Q

what is Hypohydrotic Ectodermal Dysplasia? dental relevance ?

A
  • Smooth dry skin with sparse hair
  • Partial / total absence of sweat glands
    (hypohydrotic)
  • Key dental findings include
  • Class III malocclusion
  • Anodontia / severe hypodontia
  • Deformed teeth / conical crowns
  • Delayed eruption
  • Xerostomia
  • CLP
51
Q

what is Cleidocranial Dysostosis?

A
  • Cleido - Absent / hypoplastic clavicles
  • Cranial - Fontanelles and sutures persist, helmet-like skull
  • Autosomal dominant - mutation in CBFA1/RUNX2 gene
  • Key dental findings include:
  • Class III malocclusion - Mx hypoplasia
  • Multiple supernumerary teeth
  • Dentigerous cysts
  • Retained 1ry teeth
  • Failure of eruption of 2ry teeth
52
Q
A
53
Q
A