Buerger Disease Q. 1 All of the following are the clinical feature of thromboangitis obliterans except : A Raynaud’s phenomenon B Claudication of extremeties C Absence of popliteal pulse D Migratory superficial thrombophlabitis Q. 1 All of the following are the clinical feature of thromboangitis obliterans except : A Raynaud’s phenomenon B Claudication of extremeties […]
ECTOPIC TESTIS ECTOPIA TESTIS An ectopic testicle descends normally through the inguinal canal but then moves into an abnormal position in the groin area. The main hazard is liability to injury. Sites of ectopic testis- a) Superficial inguinal pouch b) Perineum c) Root of the penis d) Femoral triangle (thigh) Ectopic testis is usually fully
ECTOPIC TESTIS Q. 1 Ectopic testis is found in all location except ‑ A Lumbar B Perineal C Intra abdominal D Inguinal Q. 1 Ectopic testis is found in all location except ‑ A Lumbar B Perineal C Intra abdominal D Inguinal Ans. C Explanation: Ans. is C Sites of ectopic testis- a) Superficial inguinal
MUCOCELE OF GALL BLADDER Mucocele of the Gall bladder It is one of the complications of Gall stones. Caused due to obstruction of the stone at the neck of the bladder. In course of time the bile is absorbed and replaced by the mucus secreted by the Gall bladder epithelium. Due to this the Gall
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Mucocele of Gall Bladder Q. 1 The treatment of choice for a mucocele of gall bladder is – A Aspiration of mucous B Cholecystectomy C Cholecystostomy D Antibiotics and observation Q. 1 The treatment of choice for a mucocele of gall bladder is – A Aspiration of mucous B Cholecystectomy C Cholecystostomy D Antibiotics and
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HEMOGLOBINOPATHIES HEMOGLOBINOPATHIES It is the family of genetic disorders caused by production of a structurally abnormal hemoglobin molecule, synthesis of insufficient quantities of normal hemoglobin, or, rarely, both. variants leading to hemoglobinopathies may be either alpha chain variants or beta chain variants. Abnormalities in the primary sequence of globin chains lead to hemoglobinopathies,e.g. HbS (qualitative hemoglobinopathy) Abnormalities in the rate
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HEMOGLOBINOPATHIES Q. 1 Sickle cell disease is: A Inherited as AR B Inherited as AD C Inherited as XLR D Inherited as XLD Q. 1 Sickle cell disease is: A Inherited as AR B Inherited as AD C Inherited as XLR D Inherited as XLD Ans. A Explanation:Inherited as AR Q. 2 Sickle cell trait
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GENE THERAPY Q. 1 Gene therapy is given in ‑ A Cystic fibrosis B Thalassemia C Sickle cell anemia D Severe combined Q. 1 Gene therapy is given in ‑ A Cystic fibrosis B Thalassemia C Sickle cell anemia D Severe combined Ans. D Explanation: Severe combined immunodeficiency [Ref KDT 6m/e p. 843, 8441 Gene
GENE THERAPY GENE THERAPY It is a technique for correcting defective gene responsible for disease development. It implies to correct the basic genetic abnormality. Gene therapy is a procedure involving inserting (or sometimes deleting) portions of gene in diseased patients for the purpose of cure. Antisense gene therapy or gene silencing selectively inactivate (or turn off)
Venous ulcers Q. 1 Complications of obesity is/are: 1. Venous ulcer 2. Pulmonary embolism 3. Pickwickian syndrome 4. Hernias 5. Pulmonary hypertension A 1,2,3 & 4 B 2,3,4 & 5 C 1,2,3 & 5 D All are true Q. 1 Complications of obesity is/are: 1. Venous ulcer 2. Pulmonary embolism 3. Pickwickian syndrome 4. Hernias
