Etiology of Malocclusions Flashcards

1
Q

what are some predisposing factors to malocclusion

A
  • disturbances in embryologic development
  • heredity
  • functional matrix- muscular or functional disturbances and habits
  • traumas- especially mandibular fractures
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2
Q

what are the primary etiologic sites and what are the diseases of each

A
  • neuromuscular system- cerebral palsy
  • bone: OI
  • teeth: ectodermic dysplasia
  • soft tissues: sclerodermia
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3
Q

what tetrogens interfere with cellular differentiation during pregnancy

A
  • alcohol
  • drugs
  • pollution
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4
Q

what is crouzon’s syndrome characterized by

A

underdevelopment of the midface and eyes that bulge from their sockets

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5
Q

how does crouzons syndrome arise

A

prenatal fusion of the superior and posterior sutures of the maxilla along the wall of the orbit

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6
Q

what are the symptoms for treacher collins

A
  • down slanting eyes with notched lower lids
  • underdevloped cheek and jawbones
  • prominent nose, broad nose and characteristically small chin with steep lower jaw angle
  • ears are malformed or prominent and hair may extend towards the face
  • hearing loss is also possible
  • may have cleft lip and/or palate, heart defects and strabismus
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7
Q

what are the symptoms of cleidocranial dysplasia

A
  • delayed closure (ossification) of the space between the bones of the skull (fontanels)
  • premature closing of the coronal suture
  • protruding jaw (mandible) and protruding brow bone (frontal bossing)
  • wide nasal bridge due to increased space between the eyes (hypertelorism)
  • high arched palate or possible cleft palate
  • short stature
  • scoliosis of the spine
  • ability to touch the shoulders together in front of the body
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8
Q

what are the dental abnormalities of cleidocranial dysplasia

A
  • failure to lose baby teeth at expected time
  • slow eruption of secondary teeth
  • extra teeth
  • absent formation of teeth
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9
Q

what type of malocclusion does OI cause

A

class III malocclusion, posterior open bite
- midline deviation, asymmetry, repercussion on the condyles
- posterior open bite: lack of chewing capability

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10
Q

what happens in DI

A

not all teeth are affected in the same manner
- if one OI member of the family has DI, all other OI member will have DI as well

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11
Q

what are the symptoms of down syndrome

A
  • underdeveloped or hypoplasia of the midfacial region
  • the bridge of the nose, bones of the midface and maxilla are relatively smaller in size
  • prognathic class III occlusal relationship which contributes to an open bite
  • molars, impacted maxillary canines, and missing premolars
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12
Q

what are facial features of cleidocranial dysplasia

A
  • wide flat forehead
  • wide set eyes
  • small sinuses
  • prolonged retention of primary teeth
  • supernumary teeth
  • severe malocclusion
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13
Q

what are the 5 clusters of phenotypic diversity

A
  • cluster 1: mild maxillary retrognathism and mandibular prognathism, flat mandibular plane
  • cluster 2: mild maxillary retrognathism and mandibular prognathism, normal mandibular plane
  • cluster 3= large mandible expressed vertically
  • cluster 4 = severely mandibular prognathic
  • cluster 5: severely maxillary retrognathic
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14
Q

what are the etiologies of deep bite and openbite

A
  • transitory
  • skeletal
  • neuromuscular imbalance: oral habits, anterior tongue posture
  • combination sleep apnea
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