儿童显性和隐性多囊肾病：通过静脉肾盂造影、超声和计算机断层扫描进行分类
Dominant and recessive polycystic kidney disease in children: classification by intravenous pyelography, ultrasound, and computed tomography.
作者信息
Kääriäinen H, Jääskeläinen J, Kivisaari L, Koskimies O, Norio R
机构信息
Children's Hospital, University of Helsinki, Finland.
出版信息
Pediatr Radiol. 1988;18(1):45-50. doi: 10.1007/BF02395759.
PMID:3277138
Abstract
Both dominant and recessive polycystic kidney disease appear in childhood. We have analyzed findings of intravenous pyelography, ultrasound and computed tomography in genetically classified cases of dominant (13 children) and recessive polycystic kidney disease (5 children) and thus defined criteria by which sporadic cases of childhood polycystic kidney disease can be classified to dominant or recessive polycystic kidney disease.
摘要
显性和隐性多囊肾病均在儿童期出现。我们分析了经基因分类的显性（13例儿童）和隐性多囊肾病（5例儿童）病例的静脉肾盂造影、超声和计算机断层扫描结果，从而确定了可将儿童期散发性多囊肾病病例分类为显性或隐性多囊肾病的标准。
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