A. Globulomaxillary cyst

B. Aneurysmal cyst

D. Dentigerous cyst

A. Hard palate

C. Tongue

D. Gingiva

A. Proteolytic chelation theory

B. Proteolytic theory

C. Autoimmune theory

A. Hypocalcified dentin

C. Dentin dysplasia

D. Dentinogenesis imperfecta

A. Dysplasia

B. Pre-cancer

C. Metaplasia

A. Plasmacytoma

B. Multiple myeloma

C. Burkitts lymphoma

D. None of the above

B. Leukoplakia

C. Oral lichen planus

D. Erythroplakia

A. Nevus

C. Fibroma

D. Pleomorphic adenoma

A. Bullous

B. Ulcerative

C. Homogenous

A. Due to irritation from calculus / over hanging restoration

C. None of the above

D. Extraction Socket

A. Nasopalatine cyst

B. Median palatine cyst

D. Globulomaxillary cyst

A. Moons molars

B. Mottled enamel

C. Turners tooth

A. Two or three years of life

B. First month of life

C. First two years of life

A. Stage III

B. Stage II

C. Stage I

A. Autosomal recessive

B. Not a inheritable trait

D. Se* linked recessive

A. Neoplastic

B. Afflicted by trauma

C. Hormonal distubance

A. Eruption hematoma

B. Capillary hemangioma

D. Cavernous hemangioma

A. Complete obstruction to minor salivary gland orifices

B. Excessive orthokeratinization of the palate

D. Diffuse parakeratinization of the palate

A. Type III dentinogenesis imperfecta

B. Type I dentinogenesis imperfecta

C. Dentin dysplasia

A. Chronic smokers

C. Excess of B-complex

D. Anti-malarial medication

A. May involve both the deciduous and the permanent dentition

C. May involve a single tooth

D. In total anodontia all teeth are missing

A. 1924

C. 1920

D. 1980

B. Black hairy tongue

C. Moellers glossitis

D. Geographic tongue

A. Congenital syphilis

B. Fluoride

C. Rickets

B. Oligodontia

C. Increased rate of caries

D. Defective enamel and dentine

A. Radiation involving normal tissues

C. Lasers

D. Chemotherapy

A. Viral

B. Endocrine

C. Injury

A. Chronic granulomatous disease

C. Inflammatory disease

D. Follilcular reticulosis

A. Palatine cyst

B. Nasopalatine cyst

C. Mid alveolar cyst

B. Turner syndrome

C. Down syndrome

D. Sturge weber syndrome

A. Gingival cyst of newborn

B. Enamel pearls

D. Epithelial rests

A. amelogenesis imperfecta

B. Odontodysplasia

D. Osteitis deformans

A. Metastatic bone disease

C. Primary hyperparathyroidism

D. Osteomalacia

A. Osteitis fibrosa cystic

B. Osteitis deformans

C. Osteoporosis

B. Upward sloping of the palpebral fissure

C. No loss of hearing

D. Progenia and mandibular prognathism

B. Vitamin A deficiency

C. Teratogens

D. Vitamin D deficiency

B. Nasopalatine cyst

C. Nasoalveolar cyst

D. Incisive canal

A. Disruption of basal lamina

B. Increase in thickness of superficial layer

D. Increase in mitotic division

B. Red spots

C. All of the above

D. Fat tissue embedded in buccal mucosa

A. Tertiary syphilis

B. Acquired syphilis

D. Secondary syphilis

B. Glossoptosis

C. Retrognathia

D. Micrognathia

A. Ventral surface

B. Posterior one third

C. Tip of tongue

A. Osteogenesis imperfecta

B. Osteopetrosis

D. Fibrous dysplasia

A. Dilaceration

B. Gemination

C. Concrescence

B. Molar region

C. Incisor region

D. Canine region

A. White spongy naevus

B. Leukemia

C. Oral hairy leukoplakia

A. Due to chronic suppurative abscess in over lying gingival tissue

C. Trauma at the time of birth

D. Severe flurosis

B. A tooth that is fractured at two or more places

C. A root or tooth that is split into two

D. Abrasions on two surfaces of single tooth

A. Dentigerous cyst, Globulomaxillary cyst, radicular cyst

B. Dentigerous cyst OKC, radicular cyst

D. B & C

A. T1 N1 Mo

B. T3 N1 Mo

C. T4 N2 Mo