New Medical MCQs – Up To Date Diseases Of Blood ( Oral Pathology And Medicine ) MCQs
This post is comprising of latest ” ( Oral Pathology And Medicine ) MCQs – Latest Competitive Medical MCQs “. Here you’ll get latest Software engineering mcqs for written test, interview with answers. If you want to improve your knowledge regarding Software engineering then read these mcqs of Design of Steel Structures.
Latest Medical MCQs
By practicing these MCQs of Diseases Of Blood ( Oral Pathology And Medicine ) MCQs – Latest Competitive Medical MCQs , an individual for exams performs better than before. This post comprising of mechanical engineering objective questions and answers related to “Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs “. As wise people believe “Perfect Practice make a Man Perfect”. It is therefore practice these mcqs of Software engineering to approach the success. Tab this page to check “Diseases Of Blood ( Oral Pathology And Medicine )” for the preparation of competitive mcqs, FPSC mcqs, PPSC mcqs, SPSC mcqs, KPPSC mcqs, AJKPSC mcqs, BPSC mcqs, NTS mcqs, PTS mcqs, OTS mcqs, Atomic Energy mcqs, Pak Army mcqs, Pak Navy mcqs, CTS mcqs, ETEA mcqs and others.
Latest Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs
The most occurred mcqs of Diseases Of Blood ( Oral Pathology And Medicine ) in past papers. Past papers of Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs. Past papers of Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs . Mcqs are the necessary part of any competitive / job related exams. The Mcqs having specific numbers in any written test. It is therefore everyone have to learn / remember the related Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs. The Important series of Diseases Of Blood ( Oral Pathology And Medicine ) Mcqs are given below:
Chediak- Higashi syndrome is inherited as_________________?
A. Autosomal dominant
B. X-linked dominant trait
C. Autosomal recessive
D. X-linked recessive
Which of the following blood disease has a racial predilection ?
A. Hemophilia
B. Purpura
C. Polycythemia
D. Thalassemia
In Radionucide imaging the most useful radio pharmaceutical for skeletal imaging is______________?
A. Technetium-99m (99m Tc-Sc)
B. Gallium 67 (67 Ga)
C. Technetium-99m (99m Tc)
D. Technetium-99m linked to Methylene disphosonate (99m Tc-MDP)
The most striking haematological finding in agranulocytosis is______________?
A. Decreased absolute neutrophil count
B. Decreased absolute basophil count
C. Increased absolute eosinophil count
D. Increased absolute monocyte count
Deficiency of all the three components of coagulation factor VIII result in_______________?
A. Von willebrand’s disease
B. Parahemophilia
C. Haemophilia- A
D. Haemophilia – B
Which of the following is not true about thalassemia ?
A. Increased in number of globulin chain
B. Hypochromic microcytic anaemia is present
C. There is erythrocyte fragility and hemolysis
D. There is severe anaemia and thrombocytopenia
A hair on end appearance of the skull is seen in all of the following except_____________?
A. Sickle anemia
B. Thalassemia
C. Cooley’s anaemia
D. Pagets disease
Hemophilia is associated with____________?
A. Prolonged bleeding time normal clotting time
B. Normal bleeding time prolonged clotting time
C. Normal bleeding time normal clotting time
D. Prolonged bleeding time prolonged clotting time
One of the following syndrome is characterized by an esophageal web with resulting dysphagia, atrophic changes in the mucous membranes of the mouth and a hypochromic microcytic anemia_____________?
A. Meckels syndrome
B. Plummer-vinson
C. Marfan’s syndrome
D. sjogren’s syndrome
Oral manifestations of infectious mononucleosis is most commonly______________?
A. Pseudomembrane on gingiva
B. Bluish red spots opposite maxillary molar
C. Pinpoint petechiae on the palate
D. Gingival hyperplasia
Chemotherapy can be successful during treatment of_____________?
A. Fibrosarcoma
B. Leukemia
C. Ameloblastoma
D. Basal cell carcinoma
Precancerous potential in plummer-vinson’s syndrome may be due to change in the epithelium like_____________?
A. Atrophy
B. Acanthosis
C. Hypertrophy
D. All of the above
Which of the following is the most serious and life threatening blood dyscrasias caused with a drug_______________?
A. Aplastic anemia
B. Thrombocytopenia
C. Megaloblastic anemia
D. Hemolytic anemia
For extraction in a leukemic patient________________?
A. Obtain WBC count
B. Consult physician
C. Obtain platelet count
D. All of the above
Plummer – vinson syndrome________________?
A. Not associated with oral premalignancy
B. common in males
C. Is due to folic acid deficiency
D. Strong association with post-cricoid carcinoma
Chronic granulocytic leukemia is due to______________?
A. Chromosomal mutation
B. Chromosomal deletion
C. Chromosomal translocation
D. None of the above
Common oral change seen with nutritional anemia is_____________?
A. Generalized osteolysis
B. Atrophic glossitis
C. Enlarged tongue
D. Focal marrow expansion
Christmas disease is due to deficiency of_______________?
A. Platelets
B. Hageman Factor
C. Plasma thromboplastin antecedent
D. Plasma thromboplastin component
Clinical features of infectious mononucleosis_________________?
A. Febrile
B. Glandular involvement
C. Palatine Petechiae
D. All of the above
Leucocytopenia is seen in________________?
A. agranulocytosis
B. influenza
C. liver cirrhosis
D. All of the above
Which of the following is not associated with haemorrhage ?
A. Petechiae
B. Ecchymosis
C. Melanosis
D. Purpura
Which of the following agents is of value in the postoperative care of the hemophilic patient ?
A. Monsel’s solution
B. Vitamin K
C. Aminocaproic acid
D. Factor 8 cryoprecipitate
A young patient is hospitalized with petechiae of oral mucous membrane, marginal gingival hemorrhage and with a platelet count of 45,000/ cc The BT and Clot Retraction time are increased, RBC and TLC are normal He is suffering from________________?
A. Thrombocytopenic purpura
B. Infectious mononucleosis
C. Leukemia
D. Hemophilia
Hemophilia B is due to______________?
A. Platelet deficiency
B. Factor IX deficiency
C. Factor VII deficiency
D. it C deficiency
Which of the following disease is known as the Kissing disease______________?
A. Primary syphilis
B. Infection mononucleosis
C. Acquired immunodeficiency syndrome (AIDS)
D. Recurrent apthous stomatitis
Neurological symptoms and premature graying of hair is associated with______________?
A. Plummer-Vinson syndrome
B. Pernicious anaemia
C. Folic acid deficiency
D. Paterson-Kelly syndrome
Hair-on-end appearance in a skull roentgenogram is seen in_______________?
A. Garre’s Osteomyelitis
B. Thalassemia
C. Fibrous dysplasia
D. Pagets disease
The oral findings in erythroblastosis fetalis include______________?
A. Hypoplastic teeth
B. Dentinal dysplasia
C. Pigmented teeth
D. All of the above
Commonest mode of inheritance of Von Willebrand’s disease is______________?
A. Autosomal recessive
B. Autosomal dominan
C. Codominant
D. X-Linked recessive
All the following are TRUE in Immune thrombocytopenic Purpura (ITP) EXCEPT_____________?
A. Increased megakaryocytes in bone marrow
B. Associated with normal bleeding time
C. Prothrombin Time (PT) & Partial Thromboplastin Time (PTT) are normal
D. Chronic ITP commonly occur in adult women
The most reliable criteria in Gustafson’s method of identification is______________?
A. Attrition
B. Transparency of root
C. Cementum apposition
D. Root resorption
The most common coagulation disorders haemophilia A and von Willebrand’s disease are due to______________?
A. Vitamin K deficiency
B. Factor IX deficiency
C. Factor X deficiency
D. Factor VIII deficiency
Cooley’s anemia is also known as_____________?
A. Aplatic anemia
B. Erythroblastosis fetalis
C. Thalassemia
D. Pernicious anemia
Erythroblastosis fetalis can be prevented if the mother is injected at parturition, with an antibody called_____________?
A. Antilymphocyte globulin
B. Rh (D) immunoglobulin
C. Blocking antibody
D. Antithymocyte serum
A patient on warfarin sodium following myocardial infarction reports for an oral surgical procedure which one of the following laboratory tests should be preferred to ascertain the fitness_______________?
A. Prothrombin time
B. Clotting time
C. Tourniquet time
D. Bleeding time
Which of the following is sex linked disorder ?
A. Klinefelter’s syndrome
B. Thalassemia
C. Hemophilia
D. Neurofibromatosis
Aplastic anaemia is common with_____________?
A. Chloramphenicol
B. Tetracycline
C. Cephalosporin
D. Penicillin
megaloblastic anaemia occurs due to________________?
A. Vitamin C deficiency
B. Folate deficiency
C. Iron deficiency
D. Protein deficiency
Virus responsible for infectious mononucleosis is_____________?
A. Varicella zoster virus
B. RNA paramyxo virus
C. Epstein Barr virus
D. Coxsackie virus A 16
Infectious mononucleosis has______________?
A. Palatal perforation
B. Ulcers which bruise easily
C. Multiple draining sinuses
D. Alveolar bone loss
Monospot test is used to diagnose_______________?
A. Sickle cell anemia
B. Pernicious anemia
C. Infectious mononucleosis
D. Leukemia
All of the following statements about acute leukemia in children are true except______________?
A. It characteristically causes gross gingival swelling
B. It can cause abvious prupura
C. It may be manifested by mucosal pallor
D. It is usually of the lymphoblastic variety
Bleeding joints is a characteristic feature of_______________?
A. Vit – K deficiency
B. Heamophilia
C. Vit – C deficiency
D. Thrombocytopenia
Hypopigmentation, gray streaks of hair, degranulation defect of neutrophils and neuropathy are seen in_____________?
A. chronic granulocytic leukemia
B. alukemic leukemia
C. lazy leukocyte syndrome
D. Chediak higashi syndrome
A boy complains of bleeding gums, swollen, joints with hemorrhage into joints His paternal and maternal uncle complains of same problem It is due to deficiency of factor________________?
A. VIII
B. X
C. IX
D. VI
Petechial hemorrhage is seen in________________?
A. agranulocytosis
B. cyclic neutropenia
C. pernicious anemia
D. thrombocytopenic purpura
Bleeding time is prolonged in_____________?
A. Henoch Schenolein purpura
B. Von Willebrand’s disease
C. Haemophilia
D. Telangiectasia
Necrotising ragged ulceration with no apparent inflammatory response is indicative of____________?
A. Polycythemia vera
B. Leucocytosis
C. Sickle cell anemia
D. Agranulocytosis
Pernicious anemia is______________?
A. can be correct by iron supplement
B. Improper maturation of red cells
C. can be correct by tablets of folic acid alone
D. insufficient production of red cells
Pinpoint hemorrhages of < 1cm diameter are known as_______________?
A. Petechiae
B. Purpura
C. Ecchymoses
D. Pustules
Paul Bunnell test is positive in______________?
A. Infectious mononucleosis
B. Malignant nerves
C. Multiple myeloma
D. Rubella
To prevent excessive bleeding during surgery a patient with hemophilia A may be given_______________?
A. Fresh frozen plasma
B. Whole blood
C. Factor VIII concentrate
D. Factor IX concentrate
Which of the following is seen in idiopathic thrombocytopenic purpura_____________?
A. Increased prothrombin time
B. Thrombocytosis
C. Increased bleeding time
D. Increased clotting time
Which of the following is not a finding in classical hemophilia (hemophilia A)_______________?
A. Decreased factor VIII
B. Bleeding into soft tissues, muscles and joints
C. Increase prothrombin Time
D. Increase Partial thromboplastin Time
The red blood cells in beta thalassemia are typically____________?
A. Normocytic and hypochromic
B. Microcytic and Hypochromic
C. Macrocytic and normochromic
D. Normocytic and normochromic
All of the following statements about idiopathic thrombocytopenic purpura are true EXCEPT________________?
A. It caused a prolonged bleeding time
B. It is associated with palatelet-specific auto-antibodies
C. It is often controlled by immunosuppressive treatment
D. It causes more prolonged hemorrhage than hemophilia