Test your basic knowledge |

Subjects : health-sciences, usmle
Instructions:
  • Answer 50 questions in 15 minutes.
  • If you are not ready to take this test, you can study here.
  • Match each statement with the correct term.
  • Don't refresh. All questions and answers are randomly picked and ordered every time you load a test.

This is a study tool. The 3 wrong answers for each question are randomly chosen from answers to other questions. So, you might find at times the answers obvious, but you will see it re-enforces your understanding as you take the test each time.
1. Cholecytsokinin - source - action - regulation






2. Where is the deep inguinal ring relative to the inferior epigastric vessels






3. misfolded gene product protein accumulates in hepatocellular ER - dec in elastic tissu in lungs leading panacinar emphysema






4. What can hemochromatosis be secondary to...






5. Gallstones that reach the common channel at ampulla can block which two ducts






6. Where does type B chronic gastritis occur and What causes it






7. What is the triad of Plummer - Vinson syndrome






8. What are the foregut structures and what supplies their blood and PANS innvervation






9. Which area of the hindgut is a watershed area






10. In what scenarios do pts with gilberts have inc bili






11. What causes carcinoid syndrome amd What are the symptoms






12. What are the branches of the celiac trunk and What do they supply






13. Bilirubin is the product of what?






14. What causes hirschsprungs






15. Which is used more quickly - an oral glucose load - or that by IV






16. GIP - source - action regulation






17. occlusion of IVC or hepatic veins






18. What transforms conjugated bilirubin to urobilinogen






19. What causes nutmeg liver






20. twisting of portion of bowel around its mesentery leading to obstruction and infarction - usually in elderly






21. What structures feed into the common hepatic duct






22. What is diverticulosis






23. What is the HLA association and treatment for hemochromatosis






24. vasoactive intestinal polypeptide (VIP) - source - action - regulation






25. What gives urine its characteristic color






26. what kind of fistula is associated with diverticulitis






27. What commonly leads to appendicity in kids vs adults






28. What does loss of p53 cause






29. AD - mutation of APC gene on chromosome 5q - two hit hypothesis - 100% progress to CRC - 1000s of polyps - pancolonic - rectal involvement






30. What is the lumen of the pancreatic duct






31. What cells secrete bicarb - What does it do - and what regulates it






32. What does the splenorenal ligament connect - and What does it contain






33. necrosis of intestinal mucosa and possible perforation - usual colon involvement - more common in preemies






34. What test and result confirms H pylori infxn






35. What histological findings are present in the esophagus






36. How is the diagonsis of CRC made






37. What do the rugae of stomach look like in menetriers disease






38. What does bicab do in the mouth






39. What serum marker increases with primary biliary cirrhosis and what other autoimmune conditions are it associated with






40. Where is bicarb trapped






41. What happens to the short gastics if the splenic artery is blocked






42. milk intolerance






43. which pancreatic enzyme - secreted in its active form - is responsible for starch digestion






44. Unencapsulated lymphoid tissue found in lamina proporia and submucosa of small intestine containing specialized M cells that take up antigen






45. strictures - fistulas - perianal disease - malabsorption - nutritional depletion - colorectal cancer






46. in jaundice of obstructive etiolgy is the hyperbilirubinemia conj or unconj - what happens to urine bili - and what happens to urine urobilinogen






47. What do tumors that arise in the head of the pancreas cause






48. What is the presenting course for appendicity


49. How do you DX and TX gallstones






50. What is the cause of physiologic neonatal jaundice