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

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