Multicystic dysplastic kidney
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
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. [1]
References
- ↑ Maria-Gisela Mercado-Deane, James E. Beeson, and Susan D. John. US of Renal Insufficiency in Neonates. RadioGraphics 2002 22: 1429-1438.
Historical Perspective
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Classification
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Pathophysiology
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Causes
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Differentiating Multicystic dysplastic kidney from other Diseases
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Epidemiology and Demographics
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Epidemiology and Demographics
In the United States, the incidence of MCDK is estimated to be 1 in every 2400 live births.[1]
References
Risk Factors
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Natural History, Complications and Prognosis
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Diagnosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Voiding Cystourethrography (VCUG) | Dimercaptosuccinic Acid (DMSA) Renal Scanning | CT | Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
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