Literature DB >> 2259758

Increased renal parenchymal echogenicity: causes in pediatric patients.

R A Kraus1, G Gaisie, L W Young.   

Abstract

The authors discuss some of the diseases that cause increased echogenicity of the renal parenchyma on sonograms in children. The illustrated cases include patients with more common diseases, such as nephrotic syndrome and glomerulonephritis, and those with rarer diseases, such as oculocerebrorenal syndrome. Hyperechogenicity is a nonspecific finding but a significant one in that it suggests the presence of renal abnormalities. When it is demonstrated, further investigation is usually warranted.

Entities:  

Mesh:

Year:  1990        PMID: 2259758     DOI: 10.1148/radiographics.10.6.2259758

Source DB:  PubMed          Journal:  Radiographics        ISSN: 0271-5333            Impact factor:   5.333


  7 in total

1.  The impact of hydration on renal measurements and on cortical echogenicity in children.

Authors:  Mooneera Peerboccus; Nasroolla Damry; Sanjiva Pather; Arnaud Devriendt; Freddy Avni
Journal:  Pediatr Radiol       Date:  2013-08-03

Review 2.  Ultrasound and color Doppler applications in chronic kidney disease.

Authors:  Ilaria Petrucci; Anna Clementi; Concetto Sessa; Irene Torrisi; Mario Meola
Journal:  J Nephrol       Date:  2018-09-06       Impact factor: 3.902

3.  Renal sonographic findings of type I glycogen storage disease in infancy and early childhood.

Authors:  Chun-Chen Lin; Jeng-Daw Tsai; Shuan-Pei Lin; Hung-Chang Lee
Journal:  Pediatr Radiol       Date:  2005-05-19

4.  Neuroimaging and renal ultrasound manifestations of Oculocerebrorenal syndrome of Lowe.

Authors:  Andrew Mark Allmendinger; Naman S Desai; Alanna Teatom Burke; Narayan Viswanadhan; Sanjay Prabhu
Journal:  J Radiol Case Rep       Date:  2014-10-31

Review 5.  Hyperechoic kidneys in the newborn and young infant.

Authors:  T L Slovis; J Bernstein; A Gruskin
Journal:  Pediatr Nephrol       Date:  1993-06       Impact factor: 3.714

6.  Abdominal ultrasonographic findings in patients with sickle-cell anaemia and thalassaemia intermedia.

Authors:  Marina G Papadaki; Antonios C Kattamis; Irene G Papadaki; Damianos G Menegas; Theano P Georgakopoulou; Anna Mavrommati-Metaxotou; Christos A Kattamis
Journal:  Pediatr Radiol       Date:  2003-06-12

7.  Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity.

Authors:  Daniela A Braun; Markus Schueler; Jan Halbritter; Heon Yung Gee; Jonathan D Porath; Jennifer A Lawson; Rannar Airik; Shirlee Shril; Susan J Allen; Deborah Stein; Adila Al Kindy; Bodo B Beck; Nurcan Cengiz; Khemchand N Moorani; Fatih Ozaltin; Seema Hashmi; John A Sayer; Detlef Bockenhauer; Neveen A Soliman; Edgar A Otto; Richard P Lifton; Friedhelm Hildebrandt
Journal:  Kidney Int       Date:  2016-02       Impact factor: 10.612

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.