A. erythema multiformae

B. Keratosis follicularils

C. lichen planus

A. Oral lichen planus

B. Aphthous stomatitis

C. Oral submucous fibrosis

A. Leukoplakia

B. Erythema multiforme

C. Pemphigus

A. Dentigerous cyst

B. Dental cyst

D. Karato cyst

A. Local alveolar osteitis

B. Condensing osteitis

D. Acute osteomyelitis

B. Leukoplakia

C. Leukoedema

D. Erythema multiformae

A. Transforms into dentigerous cyst

C. Is a type of dentigerous cyst

D. Is found in the place of the missing tooth

A. Larynx

C. Oropharynx

D. Pharynx

A. Periodontal pocket

C. Occlusal interference

D. Chronic gingivitis

A. Hereditary internal polyposis

B. Horner syndrome

D. Sturge weber syndrome

A. Von Reklinghausens neurofibromatosis

B. Albrights syndrome and Blooms syndrome

D. None of the above

A. Medial cyst

B. Follicular cyst

D. Naso labial cyst

A. Strept. mutans

C. klebsiella

D. Pneumococci

A. Hairy tongue

B. Watery saliva

C. Malignancy

A. Dentigerous cyst

B. Dermoid cyst

D. Mucocele

B. pemphigus vegentans

C. familial benign pemphigus

D. Parapemphigus

A. Craniofacial dysostosis

C. Hyperthyroidism

D. Osteitis deformans

A. Osteosarcoma

C. Metastatic carcinoma

D. Ewing sarcoma

A. Bulla

B. Macule

C. Vesicle

A. Blue

C. Yellow

D. Red

A. Streptococcus

C. Enterococcus

D. Gonococcus

B. Acute bacterial sialadenitis

C. Necrotizing sialometaplasia

D. Chronic backerial sialadenitis

A. Complete blood investigation only if adverse symptoms arise

C. No monitoring

D. Clinical observation only

A. Acanthosis of epithelium with elongation of rete ridges

B. Autosomal dominant inheritance

C. Irregular accemulation of melanin in the basal cell layer

A. High

B. Unaffected

C. Increased in morning & decrease in day

A. Primordial cyst

B. Calcifying epithelial odontogenic cyst

C. Odontoma

A. Donovan bodies

B. Tzanck cells

D. Rushton bodies

A. chronic alcoholism

B. Intercellular oedema

C. intra epithelial oedema

A. Steven-Johnson syndrome

B. ANUG

D. Herpetic stomatitis

A. Unknown compounds of phosphats

B. Potassium cloride

D. Calcium chloride

A. Wickhams Striae

C. Auspitzs sign

D. Civatte bodies

A. painless vesicular self limiting disease

B. A viral disease

C. Bacterial infection

A. IX

C. II

D. X

A. Sclerotic cemental mass

B. chronic diffuse sclerosing osteomyelitis

D. condensing osteitis

A. Acanthomatous ameloblastoma

B. Simple ameloblastoma

D. Myxoma

B. Are common cause of acute parotitis

C. Are commonest in the parotid ducts

D. Are associated with hypercaleaemic states

A. TMJ

C. sublingual salivary gland

D. Submandibular salivary gland

B. Hyperorthokeratosis

C. Hyperparakeratosis

D. Acanthosis

A. Uncontrollable twitching of muscles

B. Paralysis of one side of the face

C. Prolonged episodes of plain on one side of the face

A. Periapical cemental dysplasia

B. Familial cemental dysplasia

C. Hypercementosis

A. Multicentric reticulohisticytosis

C. Rhematoid arthritis

D. Psoriasis

B. Mac conkey medium

C. Tellurite medium

D. Nutrient agar

B. Exposure to cold

C. Local and systemic infection

D. Tooth extraction

A. Liver, spleen, pancreas

C. Parotid gland, palate, conjunctive

D. Oral mucosa, lacrimal apparatus, ears

B. Cortical bone

C. periosteum and inner cortex

D. Periosteum

A. Leukoplakia

B. Oral submucous fibrosis

C. Aphthous ulcer

A. Polyfructans

B. Lectins

D. Levans

A. Affects people in 3-4 decade of life

B. Circumscribed radio opacity

C. Continuous growth

A. Malignant melanoma

B. Squamous cell carcinoma

C. Kaposis sarcoma

A. Has associations with amelogenesis imperfecta

B. May be associated with deafness

C. In a se*-linked disorder of bones that develop that develop in cartilage