A. Can be treated with NSAIDs

B. Is a hereditary condition

D. Always bilateral in distribution

A. Ludwigs angina

B. All of the above

D. Stone or Sialolithiasis

B. Viral infection

C. Neoplastic disease

D. An inflammatory disease

B. Autosomal dominant

C. Autosomal recessive

D. X-linked dominant

B. Infectious and transmissible

C. Can develop in the absence of sucrose

D. Microorganisms play the most essential role

A. Giant cell arteritis

B. Cluster headache

D. Chronic paroxysmal hemicrania

A. herpes simplex

B. erythema multiforme

C. eipdermolysis bullosa

A. Anaerobic streptococci

B. Staphylococci

D. Legionella infection

B. Acute total pulpits

C. Acute partial pulpits

D. Strangulation of pulp

A. ? hemolytic stretococci

B. Strep. viridans

C. Non hemolytic stretococci

B. Epidermolysis bullose

C. Darier-White disease

D. Syphilis

A. Is a idiosyncrasy reaction

C. Must be excised

D. Treated only by medication

A. intake of alcohol

C. betel nut chewing

D. cigarette smoking

B. Degenerative condition

C. Reactive lesion

D. Neoplastic condition

B. Adenoid cystic carcinoma

C. Epidermoud carcinoma

D. Cylindroma

A. Abscess, cellulitis, osteitis, Periapical

C. Periapical osteitis, abscess, cellulitis,

D. cellulitis, Abscess, Periapical, osteitis

B. Loss of innervation to stapedius

C. Loss of taste sensation from Ant. 2/3 of tongue

D. Loss of lacrimal secretion

B. Mixed origin

C. Absence of capsule

D. Perineural spread

B. Phenytoin

C. Gabapentin

D. Baclofen

A. Masseter

B. Buccinator

C. Temporalis

A. Malnutrition

C. Aging

D. None of the above

A. Propranolol

B. Methysergide

D. Caffeine

A. lemphigus, CHF, diabetes

B. Hypertension with oral lesions

C. Oral, ocular, genital lesions

A. Tetanus

C. Osteomalacia

D. Multiple sclerosis

A. Sublingual nitroglycerine administration

C. Morphine administration

D. Aspirin administration

A. Horners

B. Cushins

C. Fanconis

A. Dermatitis herpetiformis

B. sarcoidosis

D. Lichen planus

B. Pierre Robin Syndrome

C. Mongolism (Downs Syndrome

D. Hypoparathyroidism

A. Apical periodontal cyst

C. Gingival cyst of new born

D. Gingival cysts of adult

A. Maxillofacial Dysostosis

B. Maxillomandibulofacial Dysostosis

D. Condylar Dysostosis

A. Cervical lymph nodes when they are enlarged due to inflammation

B. Ranula

D. Sublingual gland

A. Pemphigus

C. Leukoplakia

D. Lichen planus

A. Chronic pulpitis

B. Acute periodontal abscess

C. Cellulitis

A. Adeno carcinoma

C. Adeno cystic lymphoma

D. Pleomorphic adenoma

B. Tinels sign

C. Bablnskis sign

D. Chovsteks sign

A. Telagietasis

B. calcinosis cutis

D. Raynauds phenomenon

A. Cherubism

B. Hypophosphatasia

C. Fibrous dysplasia

A. Salivary glands

B. Teeth

D. Hair

A. Psoriasis

B. pemphigus vulgaris

C. Lupus erythematosus

D. Scleroderma

A. Rickets with involvement of teeth and bones

B. Pernicious anaemia

C. Diffuse tender ulceration on the palate predominantly

A. Apical cyst

B. Chronic apical periodontitis

C. Apical scar

A. Hemorrhagic cyst

B. Aneurysmal cyst

C. Periodontal cyst

A. Lupus erythematosus

C. pemphigus vulgaris

D. Herpangina

A. Pariapical cemential dysplasia

B. Osteoclerosis

C. Ossifying fibroma

A. Hyaluronic acid

B. Dextran

D. Amlyopecting

B. Nonspecific mumps

C. Nutritional mumps

D. Epidemic parotitis

B. No loss of muscular control

C. Bilateral involvement of the side of the face

D. Closing of the eyes

B. Tongue

C. Neck

D. Cheek

A. Glossopharyngeal neuralgia

B. Horners syndrome

C. Eagles syndrome

A. excessive salivation

B. Glossodynia

C. burning sensations in mouth