A. Dentinal dysplasia type I

B. Amelogenesis imperfecta

C. Dentinogenesis imperfecta

A. May be related to emotional stress

B. Lesions may be Bilaterally symmetrical on tongue

C. No treatment is required

A. Actinomyces

B. Strep. viridans

C. Lactobacillus

A. Focal cementoosseous dysplasia

C. Periapical cementoosseous dysplasia

D. Ossifying fibroma

A. Neuroblastoma

B. Malignant melanoma

D. Retinoblastoma

A. Permanent dentition

B. Mixed dentition

D. None of the above

A. Delayed eruption of deciduous teeth

B. Premature loss off deciduous teeth

D. Periodontal disease

A. Tetrology of fallot

B. Syndactally

D. Cleft of the lip and plate

A. Subluxation

B. None of the above

D. Dislocation

B. None of the above

C. Gemination

D. Fusion

A. Obliterated pulp chambers with secondary dentine deposition

B. Hypercementosis

C. Rootless teeth with thin shell of enamel

B. Polyostotic fibrous dysplasia

C. Pagets disease of the bone

D. Osteopetrosis

B. T2 No Mo

C. T1 N2 Mo

D. T1 NI Mo

B. Deciduous mandibular anteriors

C. Deciduous maxillary anteriors

D. Permanent manibular anteriors

A. Mandibular deciduous dentition

B. Mandibular permanent dentition

C. Maxillary deciduous dentition

A. Enbloc dissection

B. surgical excision

C. radiation

A. Adenocarcinoma

C. Squamous cell carcinoma

D. Basal cell adenoma

A. Polymerase chain reaction

C. In situ hybridization

D. Electron microscopy

A. Adenocarcinoma

B. Melanoma

C. Squamous cell carcinoma

A. Neurofibroma

C. Neuroleiomyoma

D. Trigeminal neuralgia

A. ampylobacter

B. treptococcus mutans

C. ctinomyces viscosus

D. actobacillus

B. Rickets

C. Cleidocranial Dysplasia

D. Pagets disease

A. Cilia

B. Flagella

D. Pseudopodia

A. Taurodontism

B. Enameloma

D. Ghost teeth

B. Klinefelters syndrome

C. Trisomy 21

D. Downs syndrome

A. Macrostomia

C. Ectodermal dysplasia

D. Fetal alcohol syndrome

B. Mesiodens

C. Maxillary premolars

D. Incisor with talon/cusp

A. A hereditary disturbance

B. The result of faulty enamel matrix formation

C. The result of excessive fluoride ingestion

A. Warts on the tongue

C. Cysts associated with soft palate

D. Cysts of gingiva in growing children

A. Maxillary canine

B. Paramolars

C. Paramolars

B. Tramline calcification of dura on lateral cephalogram

C. Facial hemangioma

D. Exophytic oral Hemangioma

A. Palate

C. Lateral border of tongue

D. Buccal mucosa

B. Extent

C. Pneumatization

D. Location

A. Dental Manipulation

B. Infection

D. CNS disease

A. unaffected

B. less than the patient with normal salivary flow

D. None of the above

B. Mohrs syndrome

C. Sturge-Weber Syndrome

D. Rubinstein Taybi Syndrome

A. Rickets hypomineralisation

B. Generalised dental fluorosis

D. Syphillitic hypoplasia

A. Mesiodens

B. Distal to mandibular 3rd molar

C. Para molars

B. Fusion of two teeth after calcification

C. Division of a single tooth bud after calcification

D. Fusion of two teeth before calcification

B. Availability of carbohydrate food

C. Formation of large amount of acid

D. Viscosity of saliva

A. Ectodermal dysplasia

B. Cleidocranial dysostosis

D. Osteogenesis imperfecta

A. Bilateral appearance

B. Epstein Barr virus

D. AIDS

A. Removal of adjacent teeth

C. Surgical excision

D. Irradiation of the lesion

A. Edwards syndrome

B. Downs syndrome

D. Klinefelters syndrome

A. Childhood illness

B. Osteoarthritis

C. Rheumatoid arthritis

B. Burning sensation of tongue

C. Oral cancer

D. Leukoplakia

A. Cherubism

B. Osteogenesis imperfecta

D. Fibrous dysplasia

B. CHaracteristically is columner-celled:

C. Has a recognized association with geographic tongue

D. Has a recognized association with chewing gum

A. Permanent 1st molar

B. Primary 2nd molar

C. Primary incisors

A. Concrescence

B. Twinning

C. Gemination