Polycystic kidney disease: Difference between revisions
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==Background== | ==Background== | ||
*Multisystemic and progressive disorder resulting in renal cysts and renal enlargement | *Multisystemic and progressive disorder resulting in renal cysts and renal enlargement | ||
*Hereditary disorder, autosomal dominant | |||
*Accounts for ~2% of new cases of renal failure each year | *Accounts for ~2% of new cases of renal failure each year | ||
*Mortality | *Mortality | ||
Revision as of 18:17, 28 September 2016
Background
- Multisystemic and progressive disorder resulting in renal cysts and renal enlargement
- Hereditary disorder, autosomal dominant
- Accounts for ~2% of new cases of renal failure each year
- Mortality
- Cardiovascular
- Infection, septicemia
- Subarachnoid hemorrhage
- Uremia
Clinical Features
- Clinical presentation typically begins in 3rd to 4th decade of life, but may be detectable in childhood
- Pain in abdomen/flank/back is most common initial symptom
Evaluation
- US
- BMP
References
- Torra R et al. Polycystic Kidney Disease. eMedicine. Feb 11, 2016. http://emedicine.medscape.com/article/244907-overview#showall