Severe Prenatal Renal Anomalies Associated with Mutations inHNF1BorPAX2Genes
نویسندگان
چکیده
منابع مشابه
Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
BACKGROUND AND OBJECTIVES Congenital anomalies of the kidney and urinary tract (CAKUT) are a frequent cause of renal failure in children, and their detection in utero is now common with fetal screening ultrasonography. The clinical course of CAKUT detected before birth is very heterogeneous and depends on the level of nephron reduction. The most severe forms cause life-threatening renal failure...
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ژورنال
عنوان ژورنال: Clinical Journal of the American Society of Nephrology
سال: 2013
ISSN: 1555-9041,1555-905X
DOI: 10.2215/cjn.10221012