Outcome of Multi-Cystic Dysplastic Kidneys in Children
Author | Suleiman D. Mashat | en |
Author | Sherif M. El-Desoky | en |
Author | Jameela Abdulaziz Kari | en |
Issued Date | 2015-10-28 | en |
Abstract | Background:: Renal cystic diseases are important causes of chronic kidney disease (CKD). Objectives:: We report the pattern of renal cystic disease in children and evaluate the outcome of children with multicystic dysplastic kidney (MCDK). Patients and Methods:: Retrospective study of all children with cystic kidney diseases at King Abdulaziz University hospital from 2006 to 2014. Results:: Total of 55 children (30 males); 25 MCDK, 22 polycystic kidney diseases (PKD), 4 nephronophthises and 4 renal cysts. Consanguinity was positive in 96.2%. MCDK and simple renal cyst patients had good renal function while PKD and nephronophthisis developed renal impairment. Most MCKD were diagnosed ante-natally, 16 of them were followed up for 3.4 (1.97) year. Their last creatinine was 33.9 (13.5) umol/L. MCDK was spontaneously involuted at mean age of 2.6 (1.3) years in 56%. Conclusions:: MCDK is the commonest cystic renal disease and diagnosed ante-natally in the majority of cases. It has a good prognosis. | en |
DOI | https://doi.org/10.5812/ijp.2991 | en |
Keyword | Cystic Kidney Disease | en |
Keyword | Children | en |
Keyword | Multicystic Dysplastic Kidneys | en |
Publisher | Brieflands | en |
Title | Outcome of Multi-Cystic Dysplastic Kidneys in Children | en |
Type | Research Article | en |
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