A. Penicillin

C. Co-trimoxozle

D. Clobetasol

A. Plasma thromboplastin antecedent

B. Hageman Factor

C. Platelets

A. Giant cells in the center

B. Presence of epithelioid cells

C. Central caseation

A. histoplasmosis

B. coccidiomycosis

D. cryptococcosis

A. Tongue

C. Soft palate

D. Hard palate

A. Hemophilia

B. Thrombocytopenic purpura

C. Infectious mononucleosis

D. Leukemia

A. Apical cyst

B. Chronic apical periodontitis

C. Stage one apical osteofibroses

A. Trigeminal neuraligia

B. Tuberculous meningitis

D. Rabies

B. Blood chemistry

C. Bacterial smear

D. Blood studies

A. Telangiectasia

B. Henoch Schenolein purpura

C. Haemophilia

A. Increased absolute monocyte count

B. Increased absolute eosinophil count

C. Decreased absolute basophil count

A. Routing cytology

C. Culture with giemsa stain:

D. Culture with wright strain

A. Cooleys anaemia

C. Thalassemia

D. Sickle anemia

A. Factor IX concentrate

B. Whole blood

D. Fresh frozen plasma

B. Cryptococcus neoformans

C. Aspergillosis

D. Coccidioides immitis

B. Notched incisors

C. Interstitial keratitis

D. Mulberry molars

A. Factor 8 cryoprecipitate

B. Vitamin K

D. Monsels solution

B. leishmaniasis

C. measles

D. Herpes

A. Chronic atrophic candidiasis

C. Acute pseudomembranous candidiasis

D. Acute atrohpic candidiasis

A. All of the above

B. Acanthosis

D. Hypertrophy

A. Sickle cell anemia

C. Leucocytosis

D. Polycythemia vera

A. Leprosy

B. Tetany

C. Actinomycosis

A. Actinomycosis

B. Streptococcus

D. Mycobacterium tuberulosis

A. Cementum apposition

B. Root resorption

C. Attrition

A. Alkaline phosphatase & catalase

C. Enolase & calcitonin

D. Pyrophosphatase & carbonic anhydrase

A. chronic hyperplastic candidiasis

B. Acute atrophic candidiasis

D. chronic atrophic candidiasis

A. Purpura

B. Hemophilia

C. Polycythemia

B. itching

C. painless

D. Asymptomatic

B. Bleeding time

C. Tourniquet time

D. Clotting time

A. Implicit allergic reactions

C. Recurrent allergic reactions

D. implicit bacterial infections

A. Apthous ulcer

B. Iron deficiency anaemia

D. Sickle cell anaemia

A. Prolonged tetracycline therapy

B. All of the above

C. migrating geographic tongue

A. Sjogrens disease

B. Scleroderma

D. Feltys syndrome

A. Parasitic infection

C. Fungal infection

D. Viral infection

A. Hypochromic microcytic anaemia is present

B. There is severe anaemia and thrombocytopenia

C. There is erythrocyte fragility and hemolysis

A. Tabes dorsalis

B. Gumma

C. Koplik spot

B. It can affect neonates in an epidemic fashion

C. It is characterized by a plaque of proliferating epithelial and other cells

D. It is a complication of immunosuppression or systemic diseases

B. Birth to 7th year

C. 5 months in utero to 9 months postpartum

D. 4 months in utero to 3 months postpartum

A. Leprosy

C. Cat scratch disease

D. Tuberculosis

A. Normal bleeding time normal clotting time

B. Prolonged bleeding time prolonged clotting time:

C. Prolonged bleeding time normal clotting time

A. Tuberculosis

C. Secondary herpes

D. Primary herpes

A. Macropages

C. Plasma cells

D. Eosinophils

A. Itching

B. Pain

D. Burning sensation

A. Strong association with post-cricoid carcinoma

B. Is due to folic acid deficiency

C. Not associated with oral premalignancy

B. Multiple draining sinuses

C. Palatal perforation

D. Alveolar bone loss

A. Purpura

B. Pustules

D. Ecchymoses

B. Demonstration of ray fungus in granules

C. Response to injection of vitamin B12

D. Characteristic odour

A. trophic ulcer

C. syphilitic ulcer

D. All of the above

A. pernicious anemia

B. cyclic neutropenia

D. agranulocytosis

A. Recurrent herpetiform ulcers

B. Acute herpetic gingivostomatitis

C. Recurrent aphthous minor