Chapter 6: Genetics Flashcards

0
Q

The Lyon hypothesis is demonstrated by:

A

X-linked recessive traits

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1
Q

The short and long arms of each chromosome are joined by a constriction called the:

A

Centromere

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2
Q

Trisomy is defined as:

A

A pair of chromosomes with an identical extra chromosome

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3
Q

The process by which a primitive germ cell becomes a gamete is called:

A

Meiosis

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4
Q

Barr bodies are seen at the:

A

Nuclear periphery of cells in women

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5
Q

The karyotype of a patient with Turner syndrome shows:

A

44 autosomes and XO

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6
Q

Hypothetically, an autosomal-dominant trait would be clinically present in:

A

50% of the offspring of an affected parent

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7
Q

Patients with an X-linked hereditary condition:

A

Are generally affected more severely if they are men

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8
Q

Which one of the following is associated with cyclic neutropenia?

A

Diminished number of circulating neutrophils

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9
Q

In all inherited varieties of gingival fibromatosis, the gingival enlargement is characterized by a marked:

A

Collagenization of the connective tissue

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10
Q

A 14-year-old boy is seen in consultation because of bilateral Mandibular swelling. Radiographs show a bilateral multilocular lesion in the ascending Mandibular rami. The mother of this patient has similar findings. The most likely diagnosis is:

A

Cherubism

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11
Q

A 9-year-old boy exhibits markedly swollen red and bleeding gingiva. In addition, he has tooth mobility, and the intraoral radiographs show marked alveolar bone atrophy with vertical periodontal pockets. Which of the following will be found in this child if he were to have Papillon-Lefèvre syndrome?

A

Palmar and plantar hyperkeratosis

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12
Q

Which of the following is the most serious component of Gardner syndrome?

A

Intestinal polyposis

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13
Q

A 19-year-old woman is diagnosed with cleidocranial dysplasia. She has absent clavicles and a mushroom-shaped skull. Which of the following conditions is she also most likely to have?

A

Supernumerary teeth

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14
Q

Odontogenic keratocysts are a clinical component of:

A

Nevoid basal cell carcinoma syndrome

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15
Q

Two characteristic clinical components of mandibulofacial dysostosis are:

A

Hypoplastic mandible and deafness

16
Q

Torus mandibularis and torus palatinus are:

A

Inherited as an autosomal-dominant trait

17
Q

The major concern for a dental hygienist when treating a patient with Osler-Rendu–Parkes Weber syndrome should be:

A

Gingival hemorrhage

18
Q

The cause of all forms of labial and palatal clefting is considered to be:

A

Multifactorial

19
Q

Which of the following is true for Von Recklinghausen disease?

A

Patients may have gingival neurofibromas

20
Q

The most serious clinical manifestation of the MEN 2B syndrome is considered to be:

A

Carcinoma of the thyroid gland

21
Q

Teeth in snowcapped amelogenesis imperfecta have:

A

White hypocalcified enamel at the incisal and occlusal thirds

22
Q

In dentinogenesis imperfecta type II, teeth have:

A

Roots that are short and thin

23
Q

Patients with hypohidrotic ectodermal dysplasia characteristically have:

A

Hypodontia

24
Q

Patients with hypophosphatasia characteristically have:

A

Absence of root cementum

25
Q

Taurodontic teeth:

A

Are pyramidal in shape

26
Q

The characteristic finding in permanent teeth affected with coronal dentin dysplasia is:

A

Thistle-shaped pulp chambers on radiographs

27
Q

The order of the four stages of mitosis is:

A

Prophase, metaphase, anaphase, telophase

28
Q

The so-called “enamel agenesis” is one of which type of amelogenesis imperfecta?

A

Hypoplastic

29
Q

The most frequent site of hemorrhage in patients with hereditary hemorrhagic telangiectasia is the:

A

Nasal mucosa

30
Q

The Papillon-Lefèvre syndrome is inherited according to a(n)

A

Autosomal recessive pattern

31
Q

The most frequently exfoliated teeth in patients with hypophosphatasia are the

A

Mandibular primary incisors

32
Q

Which one of the following statements is true when comparing cyclic neutropenia and Kostmann syndrome?

A

The oral lesions in Kostmann syndrome are always present unless systemic treatment is instituted

33
Q

Which of the following is a component of the Peutz-Jeghers syndrome?

A

Multiple pigmented macules on the tip of the tongue

34
Q

Radiographs of a patient with radicular dentin dysplasia show

A

Pulp chambers with a half-moon appearance