Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Multicystic dysplastic kidney
Introduction
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Overview
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.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Historical Perspective
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References
Classification
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Pathophysiology
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Causes
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References
Differentiating Multicystic dysplastic kidney from other Diseases
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References
Epidemiology and Demographics
Overview
Epidemiology and Demographics
In the United States, the incidence of MCDK is estimated to be 1 in every 2400 live births.[1]
References
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Risk Factors
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References
Natural History, Complications and Prognosis
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References
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
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]