Disturbances of the Teeth and Jaws – Exam Review

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75 question-and-answer flashcards covering disturbances of the jaws, developmental anomalies of lips, palate, and teeth, occlusal classification, enamel/dentine defects, eruption disturbances, and related syndromes to aid exam preparation.

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82 Terms

1
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What is agnathia?

A congenital absence (complete or partial) of the mandible or maxilla.

2
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Which jaw components are most often absent in mandibular agnathia?

The condyle or ramus, sometimes unilaterally.

3
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With unilateral absence of the mandibular ramus, which ear defect may be associated?

Ear deformity or agenesis.

4
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Define micrognathia.

A small-appearing jaw, usually due to abnormal jaw-to-skull relationship rather than absolute size.

5
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Name two conditions associated with true congenital mandibular micrognathia.

Pierre-Robin syndrome and certain congenital heart defects.

6
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Which joint disturbance can cause acquired micrognathia?

Temporomandibular joint ankylosis, often from trauma or infection.

7
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What is macrognathia and give one systemic cause.

Abnormally large jaws; seen in pituitary gigantism (hyperpituitarism), Paget’s disease, acromegaly, or leontiasis ossea.

8
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How does mandibular macrognathia commonly manifest radiographically?

Increased ramus height and altered ramus-body angle resulting in mandibular prognathism.

9
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What is Angle’s Class I occlusion?

Maxillary and mandibular dental arches are in normal mesiodistal relation.

10
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Describe Angle’s Class II occlusion.

The mandibular arch is distal to normal relative to the maxillary arch.

11
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Describe Angle’s Class III occlusion.

The mandibular arch is mesial to normal relative to the maxillary arch.

12
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What is facial hemihypertrophy?

Idiopathic unilateral enlargement of facial tissues, sometimes part of body hemihypertrophy.

13
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List two systemic neoplasms linked with childhood facial hemihypertrophy.

Adrenal tumors and kidney or liver neoplasms.

14
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Orally, how are permanent teeth affected in facial hemihypertrophy?

Enlarged crowns and roots with premature eruption and exfoliation.

15
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What syndrome is synonymous with facial hemiatrophy?

Parry-Romberg syndrome.

16
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Give two oral features of facial hemiatrophy.

Hollow cheek, hemiatrophy of lips/tongue, deficient root development, delayed eruption.

17
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What syndrome combines congenital lip pits with cleft lip/palate?

Van der Woude’s syndrome.

18
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Where do commissural pits occur?

At the labial commissures, uni- or bilaterally.

19
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Double lip is a feature of which syndrome?

Ascher’s syndrome (with blepharochalasis and non-toxic thyroid enlargement).

20
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State the hereditary contribution to cleft lip with/without palate.

About 40 % of cases.

21
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List three environmental factors implicated in cleft formation.

Vitamin deficiencies (A, D, E, K, B-complex), hormonal disturbances (cortisone, diabetes, thyroid disorders), infections (rubella, influenza A), radiation, drug exposure.

22
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When is surgical repair of cleft lip typically performed?

Around 1 month of age, once birth weight is regained.

23
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What is Cheilitis granulomatosa and its syndromic association?

Idiopathic diffuse lip swelling (often lower lip) linked to Melkersson-Rosenthal syndrome.

24
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Cheilitis glandularis predisposes to which malignancy?

Epidermoid carcinoma of the lips.

25
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Which intestinal polyposis syndrome shows oral mucosal pigment macules?

Peutz-Jeghers syndrome.

26
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Differentiate microdontia types.

Generalised (all teeth small) vs. focal/localised (single tooth, e.g., peg-shaped maxillary lateral incisor).

27
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Which endocrine disorder can produce generalised macrodontia?

Pituitary gigantism.

28
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Define germination in tooth development.

Partial cleavage of a single enamel organ producing two crowns sharing one root canal.

29
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How does fusion differ from germination?

Fusion is union of two separate tooth germs forming one large tooth; canals may be separate or shared.

30
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What is concrescence?

Fusion of fully formed adjacent teeth by cementum only.

31
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Dilaceration is usually caused by what?

Trauma during root development causing sharp root angulation.

32
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Describe dens invaginatus.

Invagination of enamel/dentine forming a ‘tooth-within-a-tooth,’ predisposing to pulpitis.

33
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Where are enamel pearls most often found?

Bifurcation areas of upper permanent molars below the cemento-enamel junction.

34
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What radiographic feature characterises taurodontism?

Apically displaced furcation with elongated pulp chamber (bull-like tooth).

35
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Dens evaginatus is most common on which teeth and populations?

Premolars of Asians, Inuits, and Native Americans; presents as an occlusal tubercle.

36
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Which teeth most frequently show accessory roots?

Mandibular canines, premolars, and molars (especially third molars).

37
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Define attrition.

Physiologic tooth wear from mastication, increasing with age.

38
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How does erosion differ from abrasion?

Erosion: chemical loss of tooth structure; Abrasion: mechanical wear (e.g., toothbrush).

39
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What is anodontia and its syndromic link?

Congenital absence of all teeth; often seen in ectodermal dysplasia.

40
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Name the most common congenitally missing permanent teeth in hypodontia.

Third molars, maxillary lateral incisors, and second premolars.

41
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What is a mesiodens?

A supernumerary tooth located between the maxillary central incisors.

42
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Supernumerary teeth are associated with which familial syndrome?

Gardner’s syndrome.

43
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Define natal teeth.

Structures resembling teeth present at birth, often epithelial keratinised nodules or prematurely erupted primary teeth.

44
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What is enamel hypoplasia?

Incomplete or defective enamel formation producing thin or pitted enamel.

45
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Differentiate the three clinical types of amelogenesis imperfecta.

Hypoplastic (thin enamel), hypocalcified (soft, easily removed enamel), hypomaturation (enamel pierced with explorer).

46
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Which vitamins’ deficiencies can cause environmental enamel hypoplasia?

Vitamins A, C, and D.

47
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Name three systemic conditions causing environmental enamel hypoplasia.

Exanthematous diseases (measles, chicken pox, scarlet fever), congenital syphilis, hypocalcaemia, birth injury/prematurity.

48
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What genetic defect underlies dentinogenesis imperfecta types I and II?

Mutations in COL1A1 and COL1A2 genes affecting type I collagen.

49
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Which type of dentinogenesis imperfecta is associated with osteogenesis imperfecta?

Type I.

50
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Radiographically, how do teeth appear in regional odontodysplasia?

Poorly mineralised, enlarged pulp chambers giving a ‘ghost-tooth’ appearance.

51
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What is the recommended treatment for regional odontodysplasia?

Extraction of affected teeth.

52
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Define dentine dysplasia.

Hereditary condition producing ‘rootless’ teeth due to abnormal dentine formation.

53
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List two disturbances of eruption timing.

Premature eruption, delayed eruption, impaction, ankylosed teeth.

54
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What is internal resorption of the pulp?

Progressive resorption of dentinal walls from within the pulp chamber/canal.

55
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Give two causes of external root resorption.

Trauma, orthodontic movement, cysts/tumors, impaction pressure.

56
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Differentiate exogenous and endogenous tooth stains.

Exogenous: surface discoloration from external sources (foods, tobacco). Endogenous: intrinsic discoloration from systemic factors (tetracycline, bilirubin).

57
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Which syndrome shows taurodontism together with amelogenesis imperfecta?

Hypomaturation-hypoplastic AI with taurodontism (autosomal dominant).

58
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What is flexion in root morphology?

Mild bending of tooth root, less pronounced than dilaceration.

59
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Which anomalous teeth may erupt after the permanent dentition (third dentition)?

Post-permanent supernumerary teeth (rare).

60
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Name the syndrome combining cheilitis granulomatosa, facial paralysis and fissured tongue.

Melkersson-Rosenthal syndrome.

61
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Which developmental lip disease predominantly affects males and shows everted, inflamed labial salivary glands?

Cheilitis glandularis.

62
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How are palatal clefts classified when only the uvula is split?

Isolated cleft of the uvula.

63
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Why is multidisciplinary care essential for cleft patients?

Because of combined cosmetic, feeding, speech, dental, and psychosocial issues.

64
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Which arch relationship subdivision indicates unilateral mesial positioning of the mandibular arch?

Angle’s Class III subdivision (unilaterally mesial).

65
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What oral finding is typical in hemifacial hypertrophy regarding tooth eruption timing?

Premature eruption of teeth on the affected side.

66
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A patient has bilaterally enlarged jaws due to pituitary gigantism. Which jaw condition is this?

Macrognathia affecting both jaws.

67
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Which trauma-related condition can lead to concrescence after eruption?

Post-eruption cemental fusion from trauma or overcrowding.

68
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Name two local factors that can produce environmental enamel hypoplasia of a single developing tooth.

Local infection or trauma to the primary predecessor tooth.

69
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Which developmental tooth anomaly resembles a small extra cusp on the occlusal surface of a premolar?

Dens evaginatus.

70
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Describe an enamel pearl containing a pulp horn.

A nodule of enamel with an internal dentine core and pulp horn, often at molar furcations.

71
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What is the effect of fluorosis on enamel development?

Ingestion of excessive fluoride causes environmental enamel hypoplasia with mottling and white/brown patches.

72
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Why can dilacerated roots complicate endodontic therapy?

Severe curvature makes canal instrumentation and obturation difficult.

73
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On which teeth is localized macrodontia (large single tooth) most common?

Mandibular third molars.

74
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What is the usual clinical management of an asymptomatic enamel pearl?

No treatment unless it causes periodontal problems or is caries-prone.

75
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Which developmental anomaly involves premature ankylosis of primary teeth?

Ankylosed teeth, leading to infra-occlusion and eruption disturbances of successors.

76
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How does hypocalcified AI present clinically?

Yellow-brown, soft enamel that can be scraped away easily.

77
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In which condition are blue sclerae and brittle bones seen alongside dentinogenesis imperfecta?

Osteogenesis imperfecta.

78
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What type of mutation is thought to cause regional odontodysplasia?

Somatic mutation, possibly viral in origin.

79
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Which teeth most commonly fail to develop in partial anodontia?

Third molars.

80
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What is the typical radiographic finding of dentine dysplasia (‘rootless teeth’)?

Short or absent roots with abnormal pulp chambers.

81
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List two risk factors for external chemical erosion of teeth.

Frequent citrus juice intake; gastric acid regurgitation in bulimia.

82
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Describe the occlusal effect of mandibular prognathism.

Anterior cross-bite due to forward position of the mandible relative to maxilla.