| Literature DB >> 9564103 |
K Nasu1, J Yoshimatsu, T Anai, I Miyakawa, E Komatsu, T Maeda.
Abstract
We present a case of fetal autosomal recessive polycystic kidney disease (ARPKD) at 34 weeks of gestation, diagnosed by magnetic resonance imaging (MRI). MRI demonstrated enlarged fetal kidneys that were low signal intensity on T1-weighted images and high signal intensity on T2-weighted images. These MRI findings suggested a high water content in the renal parenchyma, consistent with the innumerable, tiny renal cysts present in ARPKD.Entities:
Mesh：
Year: 1998 PMID： 9564103 DOI： 10.1111/j.1447-0756.1998.tb00049.x
Source DB: PubMed Journal: J Obstet Gynaecol Res ISSN： 1341-8076 Impact factor: 1.730