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

B. Physical form of sugar

C. Quantity of sugar intake

D. Frequency of sugar intake

A. Osteomalacia

B. condensing osteitis

C. steomyelitis

A. Apex to apex

B. Base to base

C. None of the above

A. Molybdenum

B. Strontium

C. Vanadium

A. Tissue of the odontogenic apparatus

B. Tissue of the oral mucosa

C. Infection of Salivary gland in the mandible

B. Cherubism and Polyostotic fibrous dysplasia

C. Cherubism and pagets disease

D. pagets disease and osteopetrosis

A. Fibromyoma

B. Fibrolipoma

C. Neurofibroma

B. Abnormal dentin formation in a disorganized fashion

C. Abrupt arrest to dentin formation in crown

D. Attempt to repair the defective dentin

A. Behcets

B. Reiters

D. Peutz jeghers

A. Amelogenesis imperfecta

B. Regional odontodysplasia

D. Dentinogenesis imperfecta

A. Direct textension

B. Aspiration of tumor cells

D. Blood vessels

A. Infantile skeleton

B. Prepubertal skeleton

C. Pubertal skeleton

B. Vermilion of the lip

C. Posterior tonsillar pillar

D. Palate

A. Tuberculated

B. Screw shaped

D. Incisor shaped

B. Acromegaly

C. Hyperparathyroidism

D. Fibrous dysplasia

A. Inhibitory effect on synovial membrane

B. An analgesic effects

D. Analgesic and anti-inflammatory effect

A. Benign tumour of skin and mucous membrane

C. Benign tumor of melanophores

D. Malignant tumour of melanophores

A. soluble dextan and glucosyl transferase

C. Dextranase and soluble dextran

D. None of the above

B. Erythema multiforme

C. Leukoedema

D. Oral lichen planus

A. None of the above

C. Dens is dent

D. Dentin dysplasia

B. Fibromatosis gingiva

C. Oral melanotic macule

D. Hereditary intestinal polyposis syndrome

A. Warthins tumor

B. Neurofibroma

C. Keratocanthoma

A. Shell teeth

B. Tauradontisam

C. Dentin Dysplasia