Abnormalities of Teeth Flashcards

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

A

OKC

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

A

Ankylosis

21
Q

Most commonly ankylosed tooth

A

Primary 2M

22
Q

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

A

Abrasion

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.

A

Attrition

24
Q

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

A

Abfraction

25
Q

The following conditions cause intrinsic staining of teeth:

A

Dentinogenesis imperfecta
Erythroblastosis fetalis
Porphyria
Fluorosis
Pulpal injury
Internal resorption
Tetracyclines
Hypomineralized enamel

26
Q

In an unusual form of tooth resorption that begins centrally within the tooth; endodontic therapy may be carried out

A

Internal resorption

27
Q

Extremely common and typically involved the middle or apical root. The source of resorption is in the PDL.

A

External resorption

28
Q

Type I dentin dysplasia, roots appear extremely short, and pulps are:

A

Completely obliterated

29
Q

An autosomal dominant trait that affects dentin.

A

Dentin dysplasia

30
Q

Radiographic features:

Obliterated pulp chambers and root canal
Residual fragments of pulp tissue appear typically as horizontal lucencies (chevrons)

A

Type I (radicular dysplasia) - more common type

31
Q

“Thistle tube” in appearance

A

Type II (coronal dysplasia)