- focal segmental glomerulosclerosis
- acute postinfectious glomerulonephritis
- lupus nephritis
- minimal change disease
- cirrhosis
- respiratory failure
- chronic diarrhea
- proximal renal tubular acidosis
- distal renal tubular acidosis
- maple syrup urine disease
- proximal renal tubular acidosis
- distal renal tubular acidosis
- Fanconi syndrome
- polycystic kidney disease
- diabetic ketoacidosis
- anomalous development of the urethra
- bladder thickening
- hydronephrosis
- dysplastic kidney
- XY chromosome
- ammonium chloride
- calcium glubionate
- potassium chloride
- sodium chloride
- sodium citrate
6. Prenatal ultrasonography of a male fetus reveals bilateral hydronephrosis. Postnatal abdominal ultrasonography confirms this finding, with markedly reduced renal parenchyma. A coiding cystourethrogram reveals posterior urethral valves and bilateral grade IV vesicoureteral reflux. A urologist performs ablation of the valves and bilateral ureterostomies. The infant's serum creatinine at weeks after birth is 2.1 mg/dL. The remainder of the serum electrolyte concentrations are normal, and the urine output is 5.2 mL/kg/hr. The patient has no signs of volume depletion or overload.
Of the following, the MOST appropriate statement to provide the child's parentsis that their son
- is unlikely to progress to end stage renal disease (ESRD)
- is unlikely to reach ESRD until adulthood
- likely will develop ESRD within 5 years
- needs to start peritoneal dialysis immediately
- should progress slowly to ESRD by adolescence
No comments:
Post a Comment