A. Tuberculosis

B. Lichen planus

D. Diabetes

A. X-linked recessive

B. Autosomal dominant

D. X-linked dominant trait

B. Stratum lucidum

C. Stratum spinosum

D. Stratum corneum

A. Bechets syndrome

B. Sweet syndrome

C. PFAPA (periodic fever acute pharyngitis apthous stomatitis)

A. Lips

C. Palate

D. Buccal mucosa

A. Petechiae

B. Ecchymosis

D. Purpura

A. Corynebacterium

C. Vincents angina

D. Candida

A. Increased clotting time

B. Increased prothrombin time

D. Thrombocytosis

A. Normocytic and normochromic

C. Normocytic and hypochromic

D. Macrocytic and normochromic

A. Vitamin C deficiency

C. Iron deficiency

D. Protein deficiency

A. ular (Canalicular) adenoma occurs on:

B. Burkitts lymphoma

C. Mantel cell leukemia

D. Hairy cell leukemia

B. Enlarged tongue

C. Focal marrow expansion

D. Generalized osteolysis

A. Obtain WBC count

B. Consult physician

D. Obtain platelet count

A. Increased vertical dimension

B. Recurrent herpes labialis

D. Recurrent herpetic stomatitis

B. Rasbery tongue

C. Auspitzs sign

D. Nikolskys sign

A. Fibrous dysplasia

C. Garres Osteomyelitis

D. Pagets disease

B. fibrous dysplasia

C. pyogenic granuloma

D. vincents disease

B. All of the above

C. Dentinal dysplasia

D. Hypoplastic teeth

A. Meckels syndrome

B. sjogrens syndrome

D. Marfans syndrome

A. Basal cell carcinoma

B. Ameloblastoma

C. Fibrosarcoma

A. it C deficiency

B. Factor VII deficiency

C. Platelet deficiency

A. typhoid

C. syphilis

D. measles

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