A rare cause of childhood hypertension detected in a school screening program: Answers

被引：0
作者：
Zeybek, Cengiz [1 ]
Bolat, Ahmet [2 ]
Alpman, Bedriye Nuray [1 ]
机构：
[1] Univ Hlth Sci, Gulhane Sch Med, Dept Pediat Nephrol, Ankara, Turkey
[2] Univ Hlth Sci, Gulhane Sch Med, Dept Pediat, Ankara, Turkey
来源：
PEDIATRIC NEPHROLOGY | 2021年 / 36卷 / 07期
关键词：
Child; Hypertension; Cystic kidney disease; Autosomal polycystic kidney disease; ARPKD; PKHD1; mutation; POLYCYSTIC KIDNEY-DISEASE; PKHD1; MUTATIONS; CLINICAL-EXPERIENCE; PRENATAL-DIAGNOSIS; ARPKD;
D O I：
10.1007/s00467-021-04941-z
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：2087 / 2089
页数：3
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