B. Teacher Collins

C. None of the above

D. Frey

A. Osteogenesis imperfecta

C. Osteopetrosis

D. Acromegaly

A. Ethmoid bone

B. Mandible

C. Cervical spine

A. None of the above

B. Permanent dentition

D. Mixed dentition

A. Chronic paroxysmal hemicrania

C. Giant cell arteritis

D. Cluster headache

B. Osteosarcoma

C. Ewing sarcoma

D. Metastatic carcinoma

A. Craniofacial dysostosis

B. Cleft palate

C. Cleidocranial dysplasia

A. None of the above

B. Dentin dysplasia

D. Dens is dent

A. None of the above

B. Base to base

D. Apex to apex

A. Micrognathia

B. Glossoptosis

D. Retrognathia

B. Nasopalatine cyst

C. Incisive canal

D. Nasoalveolar cyst

A. Autoimmune theory

B. Proteolytic theory

D. Proteolytic chelation theory

B. Ossifying fibroma

C. Osteoclerosis

D. Pariapical cemential dysplasia

A. Infantile skeleton

B. Prepubertal skeleton

C. Pubertal skeleton

A. Fluorides help in reducing caries incidence

B. Smooth surface caries occur due to streptococcus mutans

D. Pit and Fissure caries can be prevented by using pit and tissue sealants

A. Infiltration of eosinophils

B. Infiltration of neutrophils

C. Both of the above

A. Plasmacytoma

B. Multiple myeloma

C. Burkitts lymphoma

D. None of the above

A. Lateral pterygoid

C. Stylohyoid

D. Hyoglossus

A. Complete blood investigation only if adverse symptoms arise

B. Clinical observation only

C. No monitoring

A. Autosomal recessive

B. Not a inheritable trait

D. Se* linked recessive

A. Significant increase in number of oral bacteria

B. Significant decrease in number of oral bacteria

D. Shift towards more aerobic microflora

B. Metastatic bone disease

C. Primary hyperparathyroidism

D. Osteomalacia

A. Advancing bacteria

B. Anaerobic bacteria

D. Microcosm

A. Rootless teeth with thin shell of enamel

B. Obliterated pulp chambers with secondary dentine deposition

D. Hypercementosis

B. Cowden syndrome

C. Reiters syndrome

D. Tic doulourex

A. Squamous tissue of the mucosa

C. Connective tissue of the mucosa

D. Rests of malassez

A. Pulse granuloma

B. Bakers cyst

D. Immune granuloma

A. Maxi. Primary 1st moral

B. Mand. Primary 1st moral

C. Maxi. Primary 2nd moral

A. Always bilateral in distribution

C. Can be treated with NSAIDs

D. Is a hereditary condition

A. Moons molars

B. Turners tooth

C. Mottled enamel

A. Increase osteoclastic activity

C. Polymerisation of collagen

D. Increase fibroblastic activity

A. Glossopharyngeal neuralgia

B. Horners syndrome

C. Eagles syndrome

A. Bilateral involvement of the side of the face

C. Closing of the eyes

D. No loss of muscular control

A. Para molars

B. Distal to mandibular 3rd molar

C. Mesiodens

A. Pierre Robin Syndrome

B. Hypoparathyroidism

C. Mongolism (Downs Syndrome

A. Cherubism and pagets disease

B. pagets disease and osteopetrosis

C. Cherubism and Polyostotic fibrous dysplasia

A. Flagella

B. Pseudopodia

C. Cilia

A. Gemination

C. Concrescence

D. Dilaceration

A. Organic matrix

C. Enamel lamellae

D. Enamel cuticle

A. Irradiation of the lesion

C. Surgical excision

D. Removal of adjacent teeth

A. Recessive

B. Homozygous

D. X-linked recessive

A. Small teeth with small jaws

B. Small teeth with large jaws

C. Large teeth with small jaws

B. Fat tissue embedded in buccal mucosa

C. Red spots

D. All of the above

A. Jaffes syndrome

B. Osteogenesi imperfecta

C. Monostotic fibrous dysplasia

A. Type I

C. Type III

D. Type IIII and I

A. Flushing

C. Ptosis

D. Anhydrosis

A. Deafness

B. Multiple supernumerary teeth

D. scleroderma

B. Ostearthritis

C. Traumatic arthritis of T.M J

D. Costens syndrome

A. radiation

C. Enbloc dissection

D. surgical excision

B. Osteitis fibrosa cystic

C. Osteoporosis

D. Osteitis deformans