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Cleft Lip & Palate-overview

Apr 06, 2018

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Mohsin Habib
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    CLEFT LIP & PALATE

    - AN OVERVIEW

    Dr. Munizeh Khan

    S.R Orthodontics

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    Incidence

    1 in 500 live births

    1 in 6 children have additional malformations

    CLP: 46%

    CP: 33%

    CL: 21%

    UL > BL

    Left > Right

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    Etiology

    Syndromic

    Non-syndromic

    Environmental

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    Syndromic Clefts

    1 in 500 live births

    More than 400 syndromes associated with CLP

    Commonly associated:

    Van der Woude

    DiGeorge

    Pierre Robin sequence

    Treacher-Collins

    Stickler

    Velocardiofacial (VCFS)

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    Non-syndromic Clefts

    1 in 1000 live births

    Incidence increases with:

    Family history

    Race Negroids least affected

    Asians more commonly affected

    Afghan population shows high rate

    Gender

    Males = CLP Females = CP

    Site

    Left > Right side

    Maternal Age

    More than 38years = twice as much risk of CLP

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    Environmental Factors

    Folate deficiency

    Smoking

    Alcohol

    Epilepsy

    Drug abuse

    Medications:

    Aspirin

    Dilantin

    Valium

    6-mercaptopurine

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    Clinical Features

    Unilateral CLP:

    Flaring of unilateral alar cartilage

    Maxillary deficiency - anteroposterior

    Oronasal fistula

    Posterior crossbite

    Lack of bone support for canines and incisors

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    Clinical Features

    Bilateral CLP:

    Mobile premaxillary segment

    Flattened upper lip & philtrum

    Severe maxillary transverse deficiency

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    General Management Overview

    Immediately after birth:

    Counselling, feeding instructions

    Within first few weeks: PNAM

    Age 10-12 weeks:

    Surgical repair of cleft lip (rule of 10)

    Before age 1:

    Surgical repair of cleft palate

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    General Management Overview

    Up to 6 years of age:

    Team evaluation for speech, lip & nose revision

    Continued monitoring of ears, language, psychosocial issues

    7 years:

    Palatal expansion, Facemask therapy

    Between 9-11years:

    Alveolar bone grafting

    12 years:

    Phase II orthodontics

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    General Management Overview

    At end of orthodontic treatment:

    Placement of final prosthesis (bridge, implants etc)

    When growth is complete: Orthognathic surgery, if required

    Final lip & nose revision, if required

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    Orthodontic Intervention

    Infant orthopedics

    Primary dentition

    Mixed dentition

    Permanent dentition

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    Infant Orthopedics

    After 1-2 weeks of birth

    Appliances given to adjust position of cleft segments

    into more ideal relationship prior to definitive lip repair

    PNAM

    Active appliances

    Passive appliances

    Does not eliminate need for orthodontics

    Especially important in bilateral CLP

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    Primary dentition stage

    Caries control

    Diagnosis of developing malocclusion

    Anterior crossbite

    Equilibration

    Tongue-blade therapy, removable appliance

    Posterior crossbite

    Expansion with quad-helix or fan-shaped expander

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    Mixed dentition stage

    Incisor alignment

    Rotated, malformed, hypoplastic, malposed

    Supernumerary, absent, peg-shaped

    Maxillary expansion

    Preferable at this stage

    Quad-helix, fan-shaped

    Maxillary protraction orthopedics

    Facemask, distraction osteogenesis

    2-3 mm in 12-15 months

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    Mixed dentition stage

    Alveolar bone grafting

    Cleft alveolus

    Early = lateral incisor present, erupting Secondary = before eruption of canine

    Gold standard: autogenous bone

    Sites: iliac crest, rib, mandibular symphysis

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    Permanent dentition stage

    Management of dentition

    Align, level

    Settling of occlusion

    Space closure, prosthetic replacement

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    Permanent dentition stage

    Orthognathic surgery

    Maxilla deficient- 3 planes of space

    Mandible prognathic

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    Permanent dentition stage

    Long-term retention

    Maxillary palatal arch

    No mid-palatal suture, heavy palatal scar tissue

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