3 Written questions
3 Multiple choice questions
- 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.
- 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.
- Accumulation of fluid in the tunica vaginalis around testicle. Transilluminates well. Small ones usually spontaneously resolve within a year. Larger ones may require surgery. Seen in 2% of male neonates.
2 True/False questions
Alport syndrome → 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.
Acute glomerulonephritis → Often seen post strep infection. Common presentation is fatigue, cola-colored urine, and elevated blood pressure. Fluid intake should be restricted when oliguria is present.