Chapter 2 Flashcards

1
Q
A

Tetracycline staining

Intrinsically permanently stained - incorporated by ameloblasts

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2
Q
A

Turner’s Hypoplasia

Periapical inflammatory disease of overlying deciduous

Enamel defects of the permanent teeth

Permanent Bicuspids

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3
Q
A

Dental Fluorosis

Excess amounts of fluoride result in significant enamel defects

During tooth development (2nd and 3rd years), don’t use fluoridated toothpaste

Optimum fluoridation of drinking water –> .7ppm

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4
Q

Congenital Syphillis

A

Rare

Hutchinsons incisors

Mulberry molars

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5
Q
A

Mulberry Molars

*Congenital Syphillis*

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6
Q
A

Hutchinson’s Incisors

*Congenital Syphillis*

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7
Q

Hutchinson’s Triad

A

Hutchinson’s Teeth

Interstitial Keratitis (corneal scarring)

8th nerve deafness

Saddle nose (may manifest in leprosy as well)

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8
Q
A

Abrasion

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9
Q
A

Erosion

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10
Q
A

Abfraction

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11
Q

Impacted Teeth

A

Mandibular 3rd molars > Maxillary 3rd molars > Maxillary Canines

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12
Q
A

Ankylosis

No PDL

Fuses to the bone – WILL NOT ERUPT

Failure of the tooth to reach the occlusal plane

Primary or permanent

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13
Q

Anodontia

A

Lack of tooth development

Occur in the presence of Hereditary hpohidrotic ectodermal dysplasia (absence of ectodermal tissue development)

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14
Q

Hypodontia

A

Lack of one ore more teeth

Abscence of deciduous tooth –> Likely to miss associated permanent tooth (develop from the same dental lamina)

Ectodermal Dsyplasia –> Conical shaped teeth

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15
Q

Oligodontia

A

Lack of 6+ teeth

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16
Q

Hyperdontia

A

Supernumerary teeth

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17
Q

Mesiodens

A

supernumerary tooth that develops in the MAXILLARY incisal region between centrals

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18
Q
A

Dental Transposition

Teeth flip positions and grow not in the normal location

19
Q
A

Rege Fede Disease

Traumatic ulcerations of the adjacent soft tissue from neonatal teeth that may occur during breast feeding

20
Q

Gemination

A

Single enlarged tooth or joined teeth in which the tooth count is normal when the anomalous toot is counted as one

single pulp chamber

21
Q

Fusion

A

Single enlarged tooth or joined teeth in which the tooth count reveals a missiong tooth when the anomalous tooth is counted as one

Two different pulp chambers

22
Q

Concrescence

A

Union of two adjacent teeth by cementum alone without confluence of underlying dentin

23
Q
A

Dilaceration

A bend in the tooth – usually distally

Mandibular 3rd molars

24
Q
A

Dens Evaginatus

External growth of the tooth

PREMOLAR teeth

100% prevalence in NATIVE AMERICANS

May have a pulp horn

25
Dens - in Dente (Dens invaginatus) Deep surface invagination of the crown or rooot that is line by enamel **Permanent LATERAL incisors**
26
Taurodontium Elargement of the body and pulp chamber of a multi-rooted tooth Apical displacement of the pulpal floor Isolated or Syndromic Syndromes: \* Kleinfelter's syndrome (XXY) \* Amelogenesis imperfecta \* Trich-dento-osseous syndrome
27
Hypercementosis Non neoplastic depositio of excessive cementum - continuous with radicular cementum Threat --\> for extraction of tooth Local factors: Occlusal trauma, Adjacent inflammation Systemic Factors: Paget's Disease of bone
28
Paget's Disease of bone
Associated with generalized hypercementosis
29
30
Amelogenesis Imperfecta
AD inherited Developmental alterations of the structure of enamel No systemic disorder Permanent and Primary teeth affected
31
Hypoplastic Amelogenesis Imperfecta
Inadequate deposition of the enamel matrix Pinpoint pitting on tooth surface
32
33
Hypomaturation amelogenesis imperfecta Enamel matrix is laid down **Defect in maturation of the enamel's crystals** Snow-capped white opaque enamel on incisal or occlusal 1/3
34
Hypocalcified amelogenesis imperfecta Matrix is laid down and teeth are normal shape Enamel is soft ant is easily lost **Enamel is yellow-brown or orange - rapid calculus apposition**
35
Dentinogenesis Imperfecta **Mutation of the DSPP - dentin sialophosphoprotein gene** Primary or permanent. Blue to brown discoloration with distinctive translucence Xray: Bulbous crown, cervical constriction, thin roots, early obliteration of pulp chambers Shell teeth --\> normal thickness enamel, enlarge pulp chamber
36
Dentinogenesis imperfecta
37
Shell tooth ## Footnote **Dentinogenesis imperfecta**
38
Dentin Dysplasia
Type I and Type II Autosomal dominant
39
Dentin Dysplasia Type I **Rootless Teeth** Clinically normal -- usually mobile Enamel and coronal dentin are normal Radicular dentin looses organization and is shortened dramatically
40
Dentin Dysplasia Type 2 **Blue-Amber Brown translucence** Root length is normal Altered pulp anatomy -- thistle tube shaped teeth, pulp stones
41
Regoinal Odontodysplasia
Localized, **NON HEREDITARY** abnormality of teeth None of tooth tissues form correctly "GHOST TEETH" Usually one quadrant Clinically --\> NO TEETH PRESENT
42
Aminacycline Staining
Causes blue roots or dark crown Typically found in 3rd molars (medication taken for acne)
43
Perimolysis
Gastric Secretions Related to erosion