Abnormalities of Teeth Flashcards

(31 cards)

1
Q

The congenital absence of six or more teeth is known as:

A

Oligodontia

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2
Q

Absence of 1 or more teeth; congenitally missing teeth.

What tooth is most commonly affected?

A

Hypodontia

Third molars

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3
Q

Is having 2 successive sets of teeth (as in humans)

A

Diphyodontia

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4
Q

What is polyphyodontia?

A

Having more than 2 sets of teeth in a lifetime

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5
Q

Hypsodontia is?

A

Having teeth with high crown (cusps)

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6
Q

It is associated with a diet of abrasive food

A

Hypsodont dentition

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7
Q

What type of dentonigenesis imperfecta features multiple pulp exposures, periapical radiolucencies, and a variable radiographic appearance?

A

Type III (Brandywine type)

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8
Q

Is an autosomal dominant condition in which there is an intrinsic alteration in the dentin.

A

Dentinogenesis imperfecta

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9
Q

Dentin abnormality occurs in patient that have osteogenesis imperfecta (characterized by blue sclera or a history of bone fractures) ; PRIMARY teeth are more severely affected.

A

Dentino. Imp. Type I

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10
Q

Clinically termed as “Osteogenesis Imperfecta with opalescent teeth”

A

TYPE I D.I

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11
Q

Most common supernumerary tooth

A

Mesiodens

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12
Q

Is a developmental union of two or more teeth in which the dentin and other dental tissue are united

A

Fusion

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13
Q

Cementum of two or more teeth becomes united

A

Concrescence

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14
Q

Also called as dens invaginatus means “tooth within a tooth”; a deep invagination of the enamel organ during formation.

Most likely associated tooth?

A

Dens in dente

Maxillary lateral incisor

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15
Q

A single tooth bud attempts to divide and gives rise to the appearance of two clinical crowns

A

Gemination

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16
Q

All of the following are differential diagnoses for hypercementosis EXCEPT one.

Cemento - osseous dysplasia
Cementoblastoma
Condensing osteitis
Odontogenic keratocyst

17
Q

An enamel defect resulting from the incomplete formation of the enamel matrix is called:

A

Enamel hypoplasia

18
Q

It involves hard tissues that are derived from both epithelial (enamel) and mesenchymal (dentin and cementum); exhibits short roots, open apical foramina and enlarged pulp chambers.

A

Regional odontodysplasia

19
Q

Clinical appearance of enamel hypoplasia

A

Lack of contact between teeth
Rapid breakdown of occlusal surface
Yellowish-brown stain

20
Q

Fusion of the cementum or dentin to the surrounding alveolar bone after loss of the intervening periodontal membrane; associated with hypodontia

21
Q

Most commonly ankylosed tooth

22
Q

The abnormal loss of tooth structure due to non-masticatory physical friction is referred as:

23
Q

Is the wearing away of enamel and dentin due to the normal function or most commonly, due to excessive grinding or gritting together of teeth by patient.

24
Q

Wedge shaped cervical erosive lesion that cannot be attributed to any particular cause

25
The following conditions cause intrinsic staining of teeth:
Dentinogenesis imperfecta Erythroblastosis fetalis Porphyria Fluorosis Pulpal injury Internal resorption Tetracyclines Hypomineralized enamel
26
In an unusual form of tooth resorption that begins centrally within the tooth; endodontic therapy may be carried out
Internal resorption
27
Extremely common and typically involved the middle or apical root. The source of resorption is in the PDL.
External resorption
28
Type I dentin dysplasia, roots appear extremely short, and pulps are:
Completely obliterated
29
An autosomal dominant trait that affects dentin.
Dentin dysplasia
30
Radiographic features: Obliterated pulp chambers and root canal Residual fragments of pulp tissue appear typically as horizontal lucencies (chevrons)
Type I (radicular dysplasia) - more common type
31
“Thistle tube” in appearance
Type II (coronal dysplasia)