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3 Written Questions

3 Multiple Choice Questions

  1. Most common hereditary nephritis. Typical presentation is microscopic hematuria, especially after URI. 30 - 75% of cases are associated with progressive hearing loss. End stage renal failure is common by 20s - 30s. Usually x-linked. Ocular abnormalities may be seen, as well as rare leiomyomatosis of esophagus or respiratory tract.
  2. 8 year old with intermittent burning upon urination and trace blood on dipstick. Characterized by persistent microscopic hematuria and intermittent macroscopic hematuria. Accompanied by abdominal pain and dysuria without stone formation.
  3. Juxtaglomerular hyperplasia. Autosomal recessive. Causes hypokalemia, hypercalciuria, alkalosis, hyperaldosteronism, and hyerreninemia. Presents between 6-12 months with FTT, constipation, vomiting, polyuria, polydipsia. Treatment is fluid replacement, potassium correction, and nutrition.

2 True/False Questions

  1. Acute glomerulonephritisJuxtaglomerular hyperplasia. Autosomal recessive. Causes hypokalemia, hypercalciuria, alkalosis, hyperaldosteronism, and hyerreninemia. Presents between 6-12 months with FTT, constipation, vomiting, polyuria, polydipsia. Treatment is fluid replacement, potassium correction, and nutrition.

          

  2. Nephrotic syndrome6 year old boy with puffy eyes in the morning and scrotal swelling at night. Labs show elevated triglycerides and cholesterol. Other findings will include: low albumin, decrease in plasma volume, proteinuria. Treatment may include monitoring and salt and water restriction.

          

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