Cleft Lip and Palate Flashcards

1
Q

What are non-syndromic clefts?

A

Orofacial clefts in normal children with no other congenital deformity

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2
Q

What are some signs of syndromic orofacial clefts?

A

Mental retardation, missing fingers and toes

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3
Q

When does the development of face start and end?

A

Starts: End of 4th week of gestation

Ends: 8th week

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4
Q

What happens to the face 10th week in utero?

A

Face and palate are completely formed

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4
Q

What happens to the face 7th week in utero?

A
  1. Maxillary processes advance medially below the lateral nasal process
  2. Maxillary process will fuse with the medial nasal processes
  3. Medial nasal processes fuse with each other
  4. Complex fusion of maxillary and medial nasal processes form primary palate
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5
Q

What are the causes of a cleft?

A
  1. Hypoplasia
  2. Abnormal direction of growth of mesenchymal processes
  3. Failure of fusion
  4. Breakdown of fusion of mesenchymal process
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6
Q

What are the clinical signs of Pierre Robin syndrome?

A
  1. Mandibular hypoplasia
  2. Cleft palate
  3. Large tongue
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7
Q

What is the incidence of cleft deformity?

A

1 in 700 births

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8
Q

What is the recurrence rate of clefts?

A

Highest risk of recurrence in females with bilateral cleft lip and palate

Lowest risk of recurrence in males with unilateral CL/CP

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9
Q

What is the etiology of a cleft?

A

Interaction between genetic and environmental factors (steroids, thalidomide, alcohol, smoking, anticonvulsants)

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10
Q

What are the cleft child’s problems?

A
  1. Feeding
  2. Malocclusion
  3. Retruded maxilla/mandible
  4. Facial and other congenital deformities
  5. Speech and hearing deficiencies
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11
Q

What are the problems in feeding?

A
  1. Risk of aspiration
  2. Airway obstruction with CP and micrognathia
  3. Cleft and nasal regurgitation
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12
Q

Management of feeding problems?

A
  1. Feeding plate
  2. Soft feeding bottle with a hole and soft flange. Bottle is squeezed intermittently
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13
Q

What age is surgical correction of clefts indicated?

A

Cleft lip 3 months: 10lbs, 10mg of Hb, 10 weeks

Cleft palate 9-18 months

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14
Q

What are the type of surgeries done for Cleft lips and palates?

A
  1. Palatal lengthening/pharyngoplasty
  2. Alveolar bone grafting 7-9 years old
  3. Possible osteotomy at puberty
  4. Nose revision at puberty
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15
Q

What does the Eustachian Tube connect?

A

Connects middle ear to nasopharynx

16
Q

What are the muscles that open and close ET?

A

Tensor veli palatini and Levator veli palatini

17
Q

What is the function of ET?

A

Equalizes atmospheric pressure in middle ear

18
Q

What causes hearing deficiencies in a cleft child?

A
  1. ET malfunctions and cause pathological changes in middle ear
  2. Infection of middle ear (Otitis media)
  3. Otitis media often leads to hearing loss
19
Q

What is the management of hearing deficiencies in a cleft child?

A

Myringostomy (tympanostomy) and placement of ventilation tubes

20
Q

Why does the cleft child have speech difficulties?

A

1.Velopharyngeal mechanisms may not be adequate for normal speech

  1. May not hear well
  2. Poor dental condition
21
Q

Dental problems in cleft palate child?

A
  1. Congenitally missing teeth
  2. Supernumerary teeth
  3. Irregularities in tooth size
  4. Delayed eruption of teeth in cleft
  5. Collapsed dental arches
  6. Dental caries
22
Q

What is the role of orthodontist at the mixed dentition stage?

A

Reduce anterior cross-bites

Expand arches to correct buccal alignment

23
Q
A