A. Chlorodontia

B. Ochronosis

D. Leong teeth

A. Periodontal procedures

B. Dental extractions

C. Intracanal endodontic treatment

B. Technetium-99m (99m Tc)

C. Technetium-99m (99m Tc-Sc)

D. Gallium 67 (67 Ga)

B. Intravenous

C. Subdermal

D. Intrathecal

B. Candida albicans

C. Histoplasma capsulatum

D. Nocarda braziliances

A. Mycobacterium laprae

B. Arachnia propionica

D. Bifidobacterium dentium

A. Malignant nerves

C. Rubella

D. Multiple myeloma

B. None of the above

C. Hypoplasia of incisor and molar, V nerve motor paralysis interstitial keratitis

D. hypoplasia of incisor and molar, VIII nerve motor paralysis and peg laterals.

B. Increase Partial thromboplastin Time

C. Decreased factor VIII

D. Bleeding into soft tissues, muscles and joints

A. Vitamin K deficiency

C. Factor X deficiency

D. Factor IX deficiency

A. Chancre (primary syphilis)

C. Gumma (tertiary syphilis)

D. Congenital syphilis

A. IX

B. X

C. VI

B. life long immunity results

C. vesicles occur with both diseases

D. intranuclear inclusion bodies are present

A. Focal epithelial hyperplasia

C. Molluscum contagiosum

D. Squamous papilloma

B. Primary stage of syphilis

C. Primary tuberculosis

D. Secondary stage of syphilis

B. Diabetes mellitus

C. Local irritation

D. Pernicious anaemia

A. Cocoguesia

B. Dysguesia

D. Ageusia

A. Erosive lichen planus

B. Pemphigus vulgaris

D. Epidermolysis Bullosa

A. Apert Syndrome

B. Crounzon Syndrome

D. Downs syndrome

A. Focal periapical osteopetrosis

C. Condensing osteitis

D. Cemental dysplasia

B. Streptococcus mutans

C. Borellia vincentii

D. Staphylococci albus

A. Scarlet fever

B. Measles

D. Mumps

B. lupus vulgaris

C. Mucous patches

D. Condylomata lata

A. chronic granulocytic leukemia

C. lazy leukocyte syndrome

D. alukemic leukemia

A. It may be manifested by mucosal pallor

B. It is usually of the lymphoblastic variety

C. It can cause abvious prupura

A. Evaluation of tooth cementum annulations

B. Amino acid racemisation

D. Assessment of root dentin translucency

B. Pagets disease

C. Cleidocranial dysostoses

D. Mc Cline Albright syndrome

A. Paterson-Kelly syndrome

C. Folic acid deficiency

D. Plummer-Vinson syndrome

A. Sickle cell anemia

B. Pernicious anemia

D. Leukemia

A. None of the above

C. Chromosomal deletion

D. Chromosomal mutation

A. Coxsackie virus A 16

C. Varicella zoster virus

D. RNA paramyxo virus

A. Goblet cells

C. Pulmonary vessels

D. Pnemocyte I

A. Increased serum calcium concentration

B. Hypotonicity of muscles

C. None of the above

A. Syncope

B. Drastic fall in blood pressure

D. Precipitation of allergic reaction

A. Skeletal abnormalities of the chest

B. Asthma

D. Pulmonary artery thrombosis

A. Are under the control of parasy

B. Decrease the level o free fatty acids and ketone bodies

D. Increase the splanchnic blood flow

A. Hypoxia

C. Hypercapnia

D. Acidosis

B. Vagus nerve

C. Meissners plexus

D. Parasympathetic

B. Parathyroid hormone

C. Tumor necrosis factor

D. 1,25 dihydroxycholecalciferols

B. Sight of food

C. Food in the mouth

D. Thought of food

A. Evening

B. Sleep

C. Have no change

A. +4 mm Hg

C. -18 mm Hg

D. #NAME?

A. The gall bladder

B. Hepatic duct

D. Kupffer cells

A. decrease gastric secretion

B. neutralize the acid from the stomach

C. increase secretion of bicarbonates by pancreas

A. Dullness, loss of memory

C. Swollen, oedematous look of the face

D. Impotency, amenorrhea

A. Parathyroid hormone ( PTH)

B. Calcitonin

D. Interleukin 6 ( IL- 6)

A. Condition reflex

B. None of the above

D. Heidenhans pouch

A. Excess FSH secretion

B. Excess thyroxine secretion

C. Excess ACTH secretion

A. Causes lipogenesis

B. Secreted by beta cells

C. Promotes glycogenesis

A. Spermatogenesis

B. Sertoli cells

D. Seminiferous tubules