Facial Growth Flashcards

1
Q

Why is facial growth important?

A
  • Size, shape and position of underlying jaws determines position of teeth and therefore malocclusion
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2
Q

Why is the study of facial growth important to orthodontists?

A

Insight into growth of face so can;
- Predict changes
- Utilise growth to correct malocclusion
- Time our orthodontics and surgery

  • Understand development of facial anomalies
  • Measure changes in growth and treatment using cephalometry
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3
Q

What are the two phases of life in utero?

A

Embryonic - 1-8weeks
Foetal - 8 weeks to term

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4
Q

When can cranio-facial abnormalities form?

A
  • Very early on in pregnancy as all the limbs and organs inc face have formed within first two months
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5
Q

What time frame is the embryo most sensitive with respect to deformities?

A
  • 10% within first 4 weeks leads to miscarriages
  • Drops to 1% within 8 weeks (foetal period)
  • By end of embryonic period (8 weeks) neural tube defects drop from 2.5% to 0.1%
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6
Q

When do the neural folds fuse?

A
  • Fuse to form neural tube
  • Towards end of week 3
  • Failure to fuse will lead to spina bifida
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7
Q

What does the neural tube develop into?

A
  • Develop into brain and spinal cord
  • Failure to develop will lead to anencephaly
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8
Q

What is anencephaly?

A
  • Cerebral hemispheres and cranial vault absent
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9
Q

What do neural crest cells do?

A
  • Undergo extensive migration within developing embryo
  • Differentiate into many cell types e.g. spinal and autonomic ganglia, Schwann cells, adrenal medulla, meninges of brain
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10
Q

What does the neural crest derived ectomesenchyme do?

A
  • Contribute to branchial arch cartilage, bone and connective tissue proper
  • Also dental tissues like pulp, dentine, cementum and periodontal ligament
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11
Q

When does the formation of the face occur?

A
  • During first eight weeks after fertilisation
  • Environmental factors may lead to sig malformations in this time
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12
Q

How are defects in the face related to the brain?

A
  • Defects of face particularly in midline closely related to defects in anterior parts of brain
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13
Q

What causes severe facial deformities?

A
  • Most of face forms from migrating neural crest cells in fronto-nasal process or branchial arches
  • Interference with this causes deformities
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14
Q

What can lead to cleft formation?

A
  • Failure of fusion between various facial processes or between palatine processes
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15
Q

How can cleft lip and alveolus occur independently of cleft palate?

A
  • Upper lip and anterior part of palate have different embryological origins from posterior palate
  • Fuse at different times
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16
Q

When are the facial processes fused?

A
  • Weeks 5-7
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17
Q

What two parts are the skull divided into?

A

Neurocranium -forms protective case around brain
Viscerocranium - skeleton of face

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18
Q

What can the neurocranium be divided into?

A
  • Flat bones of vault
  • Develop intramembranously and endochondral elements of base of skull
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19
Q

What are the intramembranous bones?

A
  • Vault of skull
  • Maxilla
  • Most of mandible
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20
Q

What happens during bone formation of the intramembranous

A
  • Bone deposited into primitive mesenchymal tissue
  • Needle-like bone spicules form
  • They radiate from primary ossification centres to periphery
  • Progressive bone formation results in fusion of adjacent bony centres
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21
Q

What do the cartilages that make the base of the skull undergo?

A
  • Endochondral ossification from multiple centres
  • Starts with basi-occiput at 10-12 weeks
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22
Q

At birth where do cartilaginous growth centres remain?

A
  • Remain between sphenoid and occipital bones and nasal septum
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23
Q

When does intramembranous ossification of vault occur?

A
  • Third month
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24
Q

When does the growth of the skull stop?

A
  • Continues until 7th year
  • Some sutures remain open until adulthood
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25
Q

When do the fontanelles close and why?

A
  • Fusion incomplete at birth which leaves fontanelles to allow flexibility in skull during birth
  • Anterior fontanelle closes 2 years
  • Posterior closes 1 year
  • Growth occurs at fibrous sutures in response to intracranial pressure
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26
Q

When does maxilla and mandible form and what structures do they develop adjacent to?

A
  • Form at 6 weeks intramembranously
  • Develop next to nasal capsule and Meckel’s cartilage
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27
Q

What units is the mandible made up of?

A
  • Condylar unit
  • Angular unit
  • Coronoid unit
  • Alveolar unit
28
Q

What does the condylar unit form?

A
  • Forms articulation and contains largest secondary formation
29
Q

Why does angular unit form?

A
  • Forms in response to lateral pterygoid and masseter muscles
30
Q

Why does coronoid unit form?

A
  • Forms in response to temporalis muscle development (muscular processes)
31
Q

Why does alveolar unit form?

A
  • Only forms if teeth are developing
32
Q

Why does body of mandible form?

A
  • In response to inferior dental nerve
33
Q

What are the 3 main sites of secondary cartilage formation in mandible?

A
  • Condylar cartilage
  • Coronoid cartilage
  • Symphyseal
  • Appear between 12 and 14 weeks
34
Q

When does the coronoid cartilage disappear?

A
  • Disappears long before birth
35
Q

When does the sympheseal disappear?

A
  • Just after birth
36
Q

How long does growth of condylar cartilage continue for?

A
  • 20years of age
37
Q

At birth how does the mandible present and when does this fuse?

A
  • At birth in two halves
  • Midline symphysis fuses few months after
38
Q

What are the key bits of info for prenatal growth?

A
  • Ossification of the face and skull commences at about 7-8 weeks.
  • The neurocranium encases the brain and the viscerocranium forms the face.
  • The vault of the skull is formed intramembranously.
  • The base of skull forms by endochondral ossification.
  • Both the maxilla and the mandible develop intramembranously but are
    preceded by a cartilagenous facial skeleton.
  • Meckel’s cartilage precedes the mandible and the nasal capsule is the primary
    skeleton of the upper face
39
Q

What is the definition of primary abnormality?

A
  • Defect in structure of an organ or part of an organ that can be traced back to an anomaly in its development
  • E.g. spina bifida, cleft lip, CHD
40
Q

What is secondary abnormality?

A
  • Interruption of normal development of organ that can be traced back to other influences
  • E.g. Teratogenic agents or trauma
  • Congenital abnormality not necessarily inherited
41
Q

What is an example of teratogenic agents that can cause secondary abnormality?

A

Infection - rubella virus
Chemical - thalidomide
Chemical - lithium

42
Q

What is an example of trauma that can cause secondary abnormality?

A
  • Amniotic bands
43
Q

What is the definition of deformation?

A
  • Abnormalities that occur due to outer mechanical effects on existing structures
44
Q

What is the definition of Agenesia?

A
  • Absence of organ due to failed development during embryonic period
45
Q

What is the definition of sequence?

A
  • Single factor results in numerous secondary effects (Pierre robin)
46
Q

What is the definition of syndrome?

A
  • Group of abnormalities that can be traced to a common origin
47
Q

What are some conditions of maxillary hypoplasia?

A
  • Apert’s Syndrome* (acrosyndactyly)
  • Crouzon’s Syndrome* (craniofacial dysostosis)
  • Oral-Facial Digital Syndrome*
  • Binder’s Syndrome
  • Achondroplasia
  • Down’s Syndrome
  • Cleidocranial dysostosis*
  • Foetal Alcohol Syndrome
  • Cleft lip/palate*

*Can be associated with clefts

48
Q

What are some conditions affecting mandibular?

A
  • Treacher Collin’s Syndrome* (mandibulofacial dysostosis)
  • Pierre-Robin*
  • Stickler’s Syndrome*
  • Van der Woude Syndrome*
  • Turner’s Syndrome
  • Hemifacial Microsomia

*Can be associated with clefts

49
Q

What are some facial syndromes that can arise in first 8 weeks after conception?

A

Environmental - Foetal alcohol syndrome

Genetic

Multifactorial
- Hemifacial microsomia
- Treacher collins syndrome (mandibulofacial dysostosis)
- Clefts of lip and palate

50
Q

How does Foetal alcohol syndrome present?

A
  • Microcephaly (small head)
  • Short palpebral fissures
  • Short nose
  • Long upper lip with deficient philtrum
  • Small midface
  • Small mandible
51
Q

How and when does foetal alcohol syndrome occur?

A
  • Occurs in high maternal intake of alcohol
  • Occurs in 1:750-1000 live births
  • Microform present in 1:300 live births
  • Occurs on day 17 (very early and mother may not even know she is expecting)
52
Q

What is hemifacial microsomia?

A
  • Unilateral mandibular hypoplasia
  • Zygomatic arch hypoplasia
  • High arched palate
  • Malformed pinna
  • 3D progressive facial asymmetry
  • Normal intellect , deafness, cardiac and renal problems
53
Q

What is Treacher Collins (mandibulofacial dysostosis)?

A
  • Deformity of 1st and 2nd branchial arches (day 19-28)
  • Anti-monogloid slant palpebral fissures
  • Colomboma of lower lid outer 1/3rd
  • Hypoplastic or missing zygomatic arches
  • Hypoplastic mandible with antigonial notch
  • Deformed pinna, lead to conductive deafness
54
Q

How common is Treacher Collins (mandibulofacial dysostosis)?

A
  • 1:10,000 live births
55
Q

What is a cleft lip or palate?

A
  • When structures that form the upper lip or palate fail to join together in womb
  • Fusion of maxillary process and fused medial nasal elevation
56
Q

How common is cleft lip and/or palate?

A
  • 1:700 live births
  • 70% sporadic
  • Males > females for cleft lip and opposite for palate
57
Q

When does a cleft lip and palate occur in the womb?

A

Cleft lip = day 28-38
Cleft palate = 42-55

58
Q

What are the types of clefts lip and palate?

A
  • Normal
  • Unilateral cleft of lip extending into nose
  • Unilateral cleft lip and alveolus
  • Bilateral cleft lip and alveolus
  • Isolated cleft palate
  • Cleft palate and unilateral cleft lip
59
Q

What are the dental features of cleft lip and palate?

A
  • Impacted Teeth
  • Crowding
  • Hypodontia
  • Supernumeraries
  • Hypoplastic teeth
  • Caries
60
Q

What is Achondroplasia?

A
  • Problem with endochondrial ossification
  • Defects in long bones leading to short limbs = dwarfism in 70%
  • Defects in base of skull, retrusive middle third of face, frontal bossing, depressed nasal bridge
61
Q

What is Crouzon’s?

A
  • AKA craniofacial dysostosis
  • Premature closure of cranial suture (esp coronal and lambdoid)
  • Proptosis (shallow orbits), orbital dystopia and mild hypertelorism
  • Retrusion and vertical shortening of face
  • Prominent nose
  • Requires surgical intervention and distraction osteogenesis
62
Q

What are the dental features of Crouzon’s?

A
  • Class III malocclusion
  • Narrow spaced teeth
63
Q

What is Apert’s?

A
  • AKA Acrosyndactyly
  • Premature closure of all cranial sutures
  • Exophthalmos, hypertelorism
  • Maxillary hypoplasia
  • Parrot’s beak nose
  • Syndactyly of fingers and toes
  • Conductive deafness
64
Q

What are the dental features of Apert’s?

A
  • Class III occlusion
  • Anterior open bite (AOB)
  • Narrow spaced teeth
  • Narrow high arched palate (30% have cleft palate)
65
Q

What is hypertelorism?

A
  • Abnormally large distance between eyes
66
Q

What is exopthalmos?

A
  • Bulging or protruding of eyeball/s