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Inherited polycystic kidney disease in children.

作者信息

McDonald R A, Avner E D

机构信息

Department of Pediatrics, University of Washington School of Medicine, Seattle.

出版信息

Semin Nephrol. 1991 Nov;11(6):632-42.

PMID:1767136
Abstract
摘要

相似文献

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Inherited polycystic kidney disease in children.
Semin Nephrol. 1991 Nov;11(6):632-42.
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Early manifestations of polycystic kidney disease.
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[Gene diagnosis and clinical characteristics of autosomal recessive polycystic kidney disease].常染色体隐性遗传性多囊肾病的基因诊断与临床特征
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Perinatal differential diagnosis of cystic kidney disease and urinary tract obstruction: anatomic pathologic, ultrasonographic and genetic findings.围产期多囊肾病和尿路梗阻的鉴别诊断：解剖病理学、超声检查及遗传学发现
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[Renal polycystosis in pediatrics].[小儿肾多囊症]
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Does liver biopsy provide sufficient diagnostic information to differentiate autosomal recessive from autosomal dominant polycystic kidney disease?
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Evidence-based clinical practice guidelines for polycystic kidney disease 2014.《2014年多囊肾病循证临床实践指南》
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Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformations.一名产前检测出双侧肾囊肿且伴有多处骨骼畸形的新生儿常染色体显性多囊肾病的分子遗传学诊断
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Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4.常染色体隐性多囊肾病并不定位于4号染色体上常染色体显性多囊肾病的第二个基因位点。
Hum Genet. 1994 Jun;93(6):697-8. doi: 10.1007/BF00201574.

引用本文的文献

1
Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion.常染色体隐性多囊肾病小鼠突变体中肾脏和肝脏疾病的差异挽救。一种研究肝脏病变的新模型。
Am J Pathol. 1997 Jun;150(6):2231-41.
2
Hyperechoic kidneys in the newborn and young infant.新生儿和幼儿的高回声肾。
Pediatr Nephrol. 1993 Jun;7(3):294-302. doi: 10.1007/BF00853228.
3
Renal and biliary abnormalities in a new murine model of autosomal recessive polycystic kidney disease.常染色体隐性多囊肾病新小鼠模型中的肾脏和胆道异常
Pediatr Nephrol. 1993 Apr;7(2):163-72. doi: 10.1007/BF00864387.