ArticlePediatric nephrology (Berlin, Germany)2005
A familial case of multicystic dysplastic kidney.
Article in Pediatric nephrology (Berlin, Germany), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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6 citing papers in PubMed, 12 citations in OpenAlex.
- Sequence variants in the renin-angiotensin system genes are associated with isolated multicystic dysplastic kidney in children.Pediatric research · 2021Article
- Screening for Renal and Urinary Tract Anomalies in Asymptomatic First Degree Relatives of Children with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).Indian journal of pediatrics · 2020Article
- [Prenatal diagnosis of multicystic dysplastic kidney: about 18 cases].The Pan African medical journal · 2019Article
- Unilateral multicystic dysplastic kidney: single-center experience.Pediatric nephrology (Berlin, Germany) · 2009Article
- Are therapeutic stem cells justified in bilateral multicystic kidney disease? A review of literature with insights into the embryology.Pediatric surgery international · 2007Review
- Familial multicystic dysplastic kidney.Pediatric nephrology (Berlin, Germany) · 2005Article
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Authors and funding
11 authors at 5 institutions in 1 country.
Funding
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Abstract
A familial case of multicystic dysplastic kidney (MCDK) is described. The proband is a one-year-old boy with left MCDK, and his father was also revealed to have unilateral MCDK. The mother had two abortions; the second pregnancy was terminated because of bilateral MCDK of the fetus (Potter anomaly). The two patients and the aborted male fetus did not have any malformations except for MCDK. Thus in this family MCDK occurs as an isolated phenomenon in three individuals within two generations, presumably as a result of autosomal dominant inheritance.
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