Dental Anomalies Flashcards

1
Q

hypodontia prevelence in primary dentition

A

0.1-0.9%

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2
Q

hypodontia prevalence in permanent dentition

A

3.5-6.5%

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3
Q

conditions associated with hypodontia

A

ectodermal dysplasia
Down syndrome
cleft palate
Ellis Van Creveld syndrome
hurler’s syndrome
incontinentia pigmentii

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4
Q

Upper lateral incisor missing - possible consequence

A

over eruption of lower canine

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5
Q

Aims of hypodontia treatment

A

prevention
aesthetics
function

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6
Q

hypodontia problems

A

abnormal shape
abnormal form
spacing
infra occlusion
deep overbite
reduced LFH

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7
Q

hypodontia solutions

A

over denture
partial denture
composite
porcelain veneers
fixed prosthesis

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8
Q

prevalence of hypodontia

A

1.5-3.5%
males:females 2:1
more common in maxilla
higher frequency in Japanese
higher frequency in cleidocranial dysplasia

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9
Q

types of supernumerary

A

conical
- cone shaped
tuberculate
- barrel shaped
supplemental
- looks like tooth of normal series
odontome
- regular mass of dental hard tissue, compound or complex

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10
Q

Following removal of a supernumerary tooth, how long should you wait to allow the permanent tooth to erupt ?

A

18 months

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11
Q

anomalies of size and shape - types

A

microdontia
Microdontia
double teeth
odontomes
- complex or compound
taurodontism
- 6.3% in uK - flame shaped pulp
dilaceration
accessory cusps e.g. talon cusps

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12
Q

how are talon cusps removed?

A

selective grinding

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13
Q

anomalies of root structure examples

A

short root anomaly
- permanent maxillary incisors
radiotherapy
accessory roots

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14
Q

what is ameliogenesis imperfecta? name the types of ameliogenesis imperfecta

A

genetic enamel anomaly
affects all teeth within dentition
thin to no enamel, normal dentine and pulp
types:
hypoplastic
hypomaturational
hypocalcified
mixed forms

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15
Q

What is taurodontism?

A

vertically elongated pulp chamber and short roots
linked to type 4 ameleogenesis imperfecta

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16
Q

environmental enamel hypoplasia aetiology

A

systemic
nutritional
metabolic e.g. liver disease
infection e.g. measles

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17
Q

localised enamel hypoplasia aetiology

A

trauma
infection of primary tooth

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18
Q

what is dilaceration?

A

an abnormal bend in the root
usually due to traumatic injury to primary tooth

19
Q

localised enamel hypoplasia - questions to ask patient/parent

A
  • trauma to primary tooth
    or
  • infection in primary tooth
20
Q

generalised enamel defects - types

A

fluorosis
MIH

21
Q

fluorosis treatment

A

micro-abrasion
veneers
vital bleaching

22
Q

MIH cause

A

associated with childhood illness or chronological hypo-mineralisation e.g liver or kidney failure

23
Q

prenatal issues linked to generalised environmental enamel defects

A

rubella
congenital syphillis
thalidomide
fluoride
maternal A nd D deficiency
cardiac and kidney disease

24
Q

neonatal issues linked to generalised environmental enamel defects

A

prematurity
meningitis

25
Q

postnatal issues linked to generalised environmental enamel defects

A

otitis media
measles
chickenpox
TB
pneumonia
A, C and D deficiency
long term health problems
heart disease
diphtheria

26
Q

amelogenesis imperfecta - types

A

hypoplastic
hypocalcified
hypomaturational
mixed forms

27
Q

environmental enamel hypoplasia - causes

A

systemic
nutritional
metabolic
infection
- e.g. measles

28
Q

localised enamel hypoplasia - cause

A

trauma
infection of primary tooth

29
Q

ameliogenesis imperfecta problems

A

sensitivity
caries/acid susceptibility
poor aesthetics
poor OH - may be sensitive brushing teeth
delayed eruption
anterior open bite

30
Q

amelogenesis imperfecta diagnosis

A

family history
generally affects both dentitions
affects all teeth
tooth size, structure, colour
radiographs

31
Q

amelogenisis imperfecta - hypoplastic type

A

enamel crystals do not grow to the correct length

32
Q

amelogenesis imperfecta - hypominerilised type

A

crystallites fail to grow in thickness and width

33
Q

hypomaturational amelogenesis imperfecta

A

enamel crystals grow incompletely in thickness or width
but to normal length with incomplete mineralisation

34
Q

amelogenesis imperfecta - solutions

A

preventative therapy
composite veneers
fissure sealants
metal inlays
stainless steel crowns
orthodontics

35
Q

dentine dysplasia features

A

normal crown morphology
amber radiolucency
short constricted roots
pulpal obliteration

36
Q

What is dentinogenesis imperfecta?

A

a genetic disorder of tooth development affecting dentine

37
Q

dentinogenesis imperfecta - types

A

type 1
- osteogenesis imperfecta
type 2
- autosomal dominant
Brandywine

38
Q

dentinogenesis imperfecta - features

A

bulbous crowns
pulpal obliteration (initially large pulps)
- abscess formation
short roots

39
Q

dentinogenesis imperfecta problems

A

aesthetic
acid susceptibility
spontaneous abscess

40
Q

dentinogenesis imperfecta - solutions

A

prevention
composite veneers
over dentures
removable prostheses
stainless steel crowns

41
Q

neo-natal teeth are–

A

teeth that are present within 8 weeks of birth

42
Q

indications for extracting Neo natal teeth

A
  • poses aspiration risk
  • causes issues breastfeeding
43
Q

delayed exfoliation - potential causes

A

infra-occlusion
double primary teeth
hypodontia
ectopic permanent successors
trauma