Multicystic dysplastic kidney: Difference between revisions
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==Diagnosis== | ==Diagnosis== | ||
MCDK is usually diagnosed by [[ultrasound]] examination before birth. | MCDK is usually diagnosed by [[ultrasound]] examination before birth. | ||
==Diagnostic Findings== | |||
==Treatment== | ==Treatment== | ||
Revision as of 05:23, 12 March 2009
| Multicystic dysplastic kidney | |
| ICD-10 | Q61.4 (EUROCAT Q61.40-Q61.41) |
|---|---|
| eMedicine | radio/458 |
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Multicystic dysplastic kidney (MCDK) is a condition that results from the malformation of the kidney during fetal development. The kidney consists of irregular cysts of varying sizes and has zero function.
Epidemiology
In the United States, the incidence of MCDK is estimated to be 1 in every 2400 live births.[1]
Diagnosis
MCDK is usually diagnosed by ultrasound examination before birth.
Diagnostic Findings
Treatment
MCDK is not treatable. However, the patient is observed periodically for the first few years during which ultrasounds are generally taken to ensure the healthy kidney is functioning properly and that the unhealthy kidney is not causing adverse effects.
External links
References