PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies

2010 ◽  
Vol 80 (6) ◽  
pp. 581-585 ◽  
Author(s):  
S Negrisolo ◽  
E Benetti ◽  
S Centi ◽  
M Della Vella ◽  
G Ghirardo ◽  
...  
2006 ◽  
Author(s):  
Abdulmalik M Alkatheri ◽  
Ali Hajeer ◽  
Hanan Al Kadri ◽  
Majed Al-Jeraisy ◽  
Abullah Alsayyari

Author(s):  
Sameh Abdulsamea ◽  
William Bryant ◽  
Ben Margetts ◽  
John Booth ◽  
Stephen Marks

2008 ◽  
Vol 12 ◽  
pp. S10-S11
Author(s):  
Funda Timurkavnak ◽  
Süheyla Senger ◽  
Özlem Azap ◽  
Hande Arslan

2019 ◽  
Vol 70 (1) ◽  
pp. 83-95 ◽  
Author(s):  
Tatiana Mendonça Fazecas ◽  
Edward Araujo Júnior ◽  
Heron Werner ◽  
Pedro Daltro ◽  
Alberto Borges Peixoto ◽  
...  

Objective To assess the applicability of magnetic resonance imaging (MRI) to complement ultrasound in the diagnosis of fetal urinary tract anomalies. Methods This was a retrospective cohort study that included 41 women between 19 weeks and 37 weeks and 6 days of gestation carrying fetuses with malformations of the urinary tract which were initially diagnosed by ultrasound and then referred for MRI. In all cases, the diagnosis was confirmed after birth either through imaging or autopsy. A surface coil was positioned over the abdomen and T2-weighted sequences were obtained in the axial, coronal, and sagittal planes; T1 in at least one plane; and three-dimensional (3-D) TRUFI in fetuses with dilatation of the urinary tract. Results Mean gestational age at the time of MRI examination was 28.21 weeks. The rapid T2 sequences allowed all the anomalies of the fetal urinary tract to be assessed, whereas 3-D TRUFI sequencing proved very useful in evaluating anomalies involving dilatation of the urinary tract. The signs of pulmonary hypoplasia characterized by hypointense signal in the T2-weighted sequences were identified in 13 of the 41 fetuses. Conclusion MRI confirmed and added information to the ultrasound regarding fetal urinary tract anomalies, as well as information related to the other associated malformations, their progress in the prenatal period, and possible postnatal prognosis.


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