A. Soft palate

B. Sublingual muosa

D. Buccal mucosa

B. Acute pseudo-membranous candidiasis

C. Hemangioma

D. Focal epithelial hyperplasia

A. Leukoplakia does not disappear even after cessation of smoking

B. Oral submucous fibrosis is seen in all parts of the world

D. Leukoplakia should be proved by biopsy

A. Floor of the mouth

B. Posterior maxilla

C. Tongue

B. Bleomycosis

C. Phycomycosis

D. Actinomycosis

A. Occurs only in elderly

C. Is seen clinically as a proliferative lesion

D. Is caused by a gram -ve bacteria

A. Mucous retention cyst

B. Radicular cyst

C. Dentigetous cyst

A. Chicken pox

B. Recurrent herpes simplex infection

D. infectious mononucleosis

B. Apthous ulcers

C. Keratocyst

D. Dentigerous cyst

B. causes hypopigmentation

C. Causes hypertension

D. Steroids are contraindicated

B. Multiple myeloma

C. Squamous cell carcinoma

D. Verrucous carcinoma

A. 13-16 years

B. 6-12 years

D. They are likely to occur equally at any age

A. Small pox

B. German measles

C. Chicken pox

A. Hemangioma

C. Giant cell fibroma

D. Ameloblastoma

A. Littere Siewe Disease

C. Sickle cell anemia

D. Niemen pick disease

A. Chronic hypertrophic candidiasis

B. dental ulcers

D. Hemangioma

A. Snuff chewer

B. Cigar smoker

C. Tobacco chewer

B. Irradiation of tissues from a distance

C. Irradiation of tissues by radiopharmaceuticals

D. Irradiation of tissues from a distance of 3 cm

A. Reticuloendothelial system

C. Striated muscles

D. Smooth muscles

A. Erythema migrans

B. Chemical brun

D. Apthous ulcer

B. Are seen 2-3 days after cutaneous rashes

C. First manifestation of measles

D. Rarely seen in measles

A. Sinuses

B. Keratocytes

D. Fistulae

A. pagets disease

C. Fibrous dysplasia

D. metastatic breast carcinoma

A. Vitamin A deficiency

B. Ascorbic acid deficiency

D. Any periodontal disease

A. Osteoclastoma

B. Albrights syndrome

C. Pagets disease

B. Herpes simplex

C. Rubella

D. Cytomegalovirus

A. Tip of tongue

B. Posterio 1/3

D. Ventral surface

A. submental and submandibular lymphnodes

B. Jugulo omohyoid and jugulo digastric

D. None of the above

A. Aphthous ulcers

B. Lesions of Behcets syndrome

C. koplick spots

B. Leprosy

C. Syphilis

D. Tuberculosis

A. Atrophy of filiform papillae

B. Hypertrophy of filiform papillae

C. Inflammation of the tonge

A. Metaplasia

B. Granular cell myoblastoma

C. Neurofibroma

A. citric acid

B. phytates

D. Oxalates

A. Papilloma

B. Fibroma

D. Rhabdomyoma

A. Dentin deficiency

B. Material alba

C. Enamel deficiency

A. Etiological agents differ

C. The patient has received antibodies during intrauterine life and the antibodies have persisted

D. The acute form occurs only inversely immuno compromised individuals

B. Juvenile periodontitis

C. Osteomalacia

D. Vit. D resistant Rickets

B. Herpes simplex

C. Poliomyelitis

D. chicken pox

A. Bacteriophages

B. Donavan bodies

D. Negri bodies

B. Rare in children

C. Palate is the most common intraoral site

D. Is very painful

A. Kidney

B. Lung

D. Prostatic

A. Marfans syndrome

C. Cushings syndorme

D. Multiple myeloma

A. None of the above

C. fibrous dysplasia

D. Addisons disease

A. Crowded teeth

C. Large tongue

D. Micrognathia

A. pemphigus

B. erythema multiforme

D. pemphigoid

B. Neurogenic fibroma

C. Traumatic neuroma

D. Neurolemmoma

A. Freckle

B. Cafe-au-lait-spots

C. Melanoma

A. Glandular fever

B. Hansans disease

D. Alpha-thalassemia

A. Oral submucous fibrosis

C. Atrophic glossitis

D. Syphilitic glossitis

B. Niacin

C. Pantothenic acid

D. Vitamin B