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Pedo2013-14

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    PEDI TRIC DENTISTRY

    Topic

    Cards

    LEG ND

    Topic

    abnormal teeth

    1 4

    primary dentition

    behavior management

    5 10

    pulp treatment

    diseases

    conditions

    11 31

    restorative

    drugs

    32 34

    tooth development

    fluoride

    35 43

    tooth trauma

    general information

    44 57

    space management

    miscellaneous

    58 60

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    abn of teeth

    Radiographs of a preschool child with

    will show obliteration

    of the pulp chambers with secondary dentin, a characteristic finding.

    amelogenesis imperfecta

    dentinogenesis imperfecta

    fluorosis

    enamel hypoplasia

    copyright 2013-2014 - Dental Decks

    PEDIATRIC DENTISTRY

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    dentinogenesis imperfecta

    Dentinogenesis imperfecta

    (DI) is an autosomal dominant trait, its frequency of occurrence is about I in 8000.

    This inherited dentin defect originates during the histodifferentiation stage of tooth development. The predentin

    matrix is defective resulting in amorphic, disorganized, and atubular circumpulpal dentin. Teeth are blue-gray

    or brown and abrade rapidly. Occasionally, these teeth become abscessed as a result of exposure of pulp horns

    caused by w ear. Full coverage is the treatment of choice. Both the primary and permanent den titions are affected

    in dentinogenesis imperfecta. Important: Radiographs of a preschool child with dentinogenesis imperfecta will

    show obliteration of the pulp

    chambers with secondary dentin, a characteristic finding. Roots of teeth usually

    are narrower and appear more fragile. Crowns generally appear more bulbous than usual due to the smaller

    roots. Dentinogenesis imperfecta can be subdivided into three basic types:

    Shields Type I:

    occurs with osteogenesis imperfecta. As a result of an inherited defect in collagen forma-

    tion, there is brittle bones, bowing of the limbs, and blue sclera. Periapical radiolucencies, bulbous crowns,

    obliterated pulp chambe rs, and root fractures are common. Teeth hav e

    amber translucent color. Primary teeth

    affected more than perma nent teeth.

    Shields Type II:

    also known as

    hereditary opalescent

    dentin, tends to occur as a separate entity apart from

    osteogenesis imperfecta. Same characteristics as Type I. Both primary a nd perma nent teeth affected equally.

    Shields Type III: quite rare, demonstrates teeth with a shell-like appearance and multiple pulp exposures.

    Seen exclusively in a triracial isolated group in Maryland known as the Brandywine population.

    Amelogen esis imperfecta is one of the m ajor defects of enamel. It is a hereditary disease characterized by faulty

    development of the enamel. There is normal pulpal and root morphology. There are four major categories ac-

    cording to the stages of tooth developm ent in which each is thought to occu r.

    Hypoplastic Type: occur in the histodifferentiation stage of tooth development. There is an insufficient

    quantity of enamel formed due to areas of the enamel organ that are devoid of inner enamel epithelium, caus-

    ing a lack o f cell differentiation into ameloblasts. Affects both primary a nd perm anent dentitions. The affected

    teeth appear small with open contacts; clinical crowns contain very thin or nonexistent enamel.

    Hypomaturation Type: defect in enamel matrix apposition and is characterized by teeth having normal

    enamel thickness but a low va lue of radiodensity and mineral content.

    Hypoplastic or Hypom aturation Type

    with Taurodontism: is an example of inherited defects in both

    ap-

    position and histodifferentiation stages in enamel formation. The enamel appears mottled with a yellow-

    brown color and is pitted on the facial surfaces. Molar teeth demo nstrate taurodontism.

    Hypocalcification Type: is an example of inherited defect in the calcification stage of enamel formation.

    Quantitatively, the enamel is normal, but qualitatively, the matrix is poorly calcified. The enamel is soft and

    fragile and is easily fractured., exposing the underlying dentin, which produces an unesthetic appearance.

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    abn of teeth

    is a process in which a single tooth germ splits or shows an

    attempt at splitting to form two completely or partially separated crowns.

    concrescence

    gemination

    fusion

    dens in dente

    copyright 2013-2014 - Dental Decks

    PEDIATRIC DENTISTRY

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    gemination

    Gemination is a process in which a single tooth germ splits or shows an attempt at splitting to form two

    completely or partially separated crowns. This process results in incomplete formation of two teeth. Like

    fusion, it is also more common in the primary dentition. It results in a bifid crown with a single pulp

    chamber. It most frequently occurs in the incisor region. Concrescence

    is a twinning anomaly involv-

    ing the union of two teeth by cem entum only. Its etiology is thought to be trauma or adjacent tooth mal-

    position.

    The term dens-in-dente (also called dens invaginatus)

    means a

    tooth within

    a tooth and results from

    the

    invagination

    of the inner enamel epithelium. Most frequently involves the maxillary lateral inci-

    sors. The clinical significance of this anomaly results from potential carious involvement through com-

    munication of the invag inated portion of the lingual surface of the tooth with the outside environm ent.

    The enam el and dentin in the invaginated portion can be both defective and absent, allowing direct ex-

    posure of the pulp.

    Dens evaginatus

    is an extra cusp, usually in the central groove or ridge of a posterior tooth and in the

    cingulum area of central and lateral incisors. In incisors, these cusps appear talon-shaped.

    It results

    from the evagination

    of inner ename l epithelial cells. This extra portion contains not only enam el but

    also dentin and pulp tissue; therfore, care must be taken with any operative procedure.

    Fusion of teeth is a condition produced when two tooth buds are joined together during development and

    appear as a macrodont (a single large crown). It is more comm on in the primary dentition. It may involve

    the entire length of two teeth

    (enamel, dentin, and cementum)

    or just the root

    (dentin and cementum). This

    condition is usually seen in the incisor area. Although fused teeth can contain two separate pulp cham -

    bers, many appe ar as large bifid crowns with one cham ber.

    Note: A radiograph is needed to confirm

    whether there is fusion or gemination.

    1 Taurodont teeth are characterized by a significantly elongated pulp cham ber with short

    Notes

    stunted roots resulting from the failure of the proper level of horizontal invagination of Her-

    twig epithelial root sheath.

    2

    Dilaceration refers to an abnormal bend of the root during its development;

    it is thought

    to result from a traumatic episode, usually to the primary dentition. It is a consistent finding

    in children with congenital ichthyosis.

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    enamel hypoplasia

    erythroblastosis fetalis

    nursing bottle caries

    dentinal dysplasia

    abn of teeth

    What condition is depicted below?

    Copyright 2000-2004 University of Washington. All rights reserved. Access t


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