Orofacial Clefts Flashcards

1
Q

What is orofacial cleft?

A
  • Failure of lip and palate tissues to close during embryonic development
  • Present at birth
  • Malformation, deformation, or disruption in one or more parts of the body
  • Has a serious, adverse effect on health, development, or functional ability
  • Most common: in American indians, Whites, Asains
  • Least Common: African Americans
  • Males: Lip and palate (mostly)
  • Females: Cleft palate only
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2
Q

What are the causes of nonsyndromic (isolated) cleft ?

A
  • inherited (Genetics)
  • Environmental (Teratogens): Gestational diabetes
  • Protective: maternal education level of bachelors degress and prenatal care
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3
Q

What are the causes of syndromic clefts?

A
  • Associated with other congenital disorders or syndromes
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4
Q

What are the causes of pierre robin sequence?

A
  • Cleft palate
  • Micrognathia (small mandible)
  • Glossopotosis (airway obstruction caused by
    tongue displacement).
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5
Q

What is the embryology ?

A

Upper lip forms 5th week
Palate forms 5-12 week

Lip Cleft: Chelioschisis
Palate Cleft: Palatoschisis

Fusion failure: late movement of lateral palatine process

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6
Q

What orofacial clefts ais most severe?

A

Bilateral complete CLP

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7
Q

What are the medical management ?

A

Primary Surgery / Repair
* Chelioplasty between 3-12 months
* Palatoplasty between 9-18 months
* Nasoalveolar molding appliance

Oral Appliances
* Obturators, palatal lift, speech bulb

Secondary
* Cosmetic, reconstructive, orthognathic

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8
Q

What are the dental management ?

A

Collaboration with interprofessional team

Educate and understand complications

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9
Q

What are the oral manifestations?

A

Malocclusion Class III

Open palate

Maxillary growthrestriction

Congenitally missing and supernumerary teeth

Teeth morphologically deformed, hypoplastic,
hypomineralized

Increase caries risk in primary dentition
(maxillary incisors, teeth adjacent to cleft, molars)

Oral prostheses effects: gingival
inflammation, recession

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