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A 7-year-old girl with renal medullary hyperechogenicity and hypertension: Answers.

作者信息

Girişgen İlknur, Yüksel Selcuk, Ufuk Furkan, Durak Taner, Becerir Tülay

机构信息

Department of Pediatric Nephrology, Faculty of Medicine, Pamukkale University, Kınıklı Campus, 20070, Denizli, Turkey.

Department of Pediatric Nephrology and Rheumatology, Faculty of Medicine, Pamukkale University, Kınıklı Campus, 20070, Denizli, Turkey.

出版信息

Pediatr Nephrol. 2022 Jan;37(1):135-138. doi: 10.1007/s00467-021-05314-2. Epub 2021 Oct 11.

DOI:10.1007/s00467-021-05314-2
PMID:34633535
Abstract
摘要

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本文引用的文献

1
Hypertension in a patient with medullary sponge kidney: A case report.海绵肾患者的高血压：病例报告。
Medicine (Baltimore). 2021 Jan 22;100(3):e24305. doi: 10.1097/MD.0000000000024305.
2
Predictors of progression in autosomal dominant and autosomal recessive polycystic kidney disease.常染色体显性遗传多囊肾病和常染色体隐性遗传多囊肾病进展的预测因素。
Pediatr Nephrol. 2021 Sep;36(9):2639-2658. doi: 10.1007/s00467-020-04869-w. Epub 2021 Jan 21.
3
Long-term kidney and liver outcome in 50 children with autosomal recessive polycystic kidney disease.
50 例常染色体隐性遗传性多囊肾病患儿的长期肾脏和肝脏预后。
Pediatr Nephrol. 2021 May;36(5):1165-1173. doi: 10.1007/s00467-020-04808-9. Epub 2020 Nov 9.
4
Hereditary Renal Cystic Disorders: Imaging of the Kidneys and Beyond.遗传性肾囊性疾病：肾脏及其他部位的影像学表现
Radiographics. 2017 May-Jun;37(3):924-946. doi: 10.1148/rg.2017160148.
5
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.序列变异解读的标准与指南：美国医学遗传学与基因组学学会和分子病理学协会的联合共识推荐
Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.
6
Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney disease.73 例常染色体隐性多囊肾病患者的肾功能、体积和影像学表现与 PKHD1 突变的相关性。
Clin J Am Soc Nephrol. 2010 Jun;5(6):972-84. doi: 10.2215/CJN.07141009. Epub 2010 Apr 22.
7
An unusual case of renal medullary hyperechogenicity and hypertension. Autosomal recessive polycystic kidney disease (ARPKD).一例罕见的肾髓质高回声与高血压病例。常染色体隐性多囊肾病（ARPKD）。
Pediatr Nephrol. 2009 Aug;24(8):1473-6. doi: 10.1007/s00467-008-1071-z. Epub 2008 Dec 13.
8
Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease.常染色体显性和常染色体隐性多囊肾病的基因型-表型相关性
J Am Soc Nephrol. 2007 May;18(5):1374-80. doi: 10.1681/ASN.2007010125. Epub 2007 Apr 11.
9
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).PKHD1基因的多外显子缺失导致常染色体隐性多囊肾病（ARPKD）。
J Med Genet. 2005 Oct;42(10):e63. doi: 10.1136/jmg.2005.032318.
10
High-resolution renal sonography in children with autosomal recessive polycystic kidney disease.
AJR Am J Roentgenol. 2005 May;184(5):1630-3. doi: 10.2214/ajr.184.5.01841630.