Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping
Glomerular diseases (GDs) are a major cause of chronic kidney disease in children. The conventional approach to diagnosis of GDs includes clinical evaluation and, in most cases, kidney biopsy to make a definitive diagnosis. However, in many cases, clinical presentations of different GDs can overlap,...
Saved in:
Main Authors: | Reeti Kumar (Author), Vahakn Keskinyan (Author), Megan Chryst Stangl (Author), Brandon M. Lane (Author), Anne F. Buckley (Author), Laura Barisoni (Author), David N. Howell (Author), Rasheed A. Gbadegesin (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2022-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population
by: Jennifer D. Varner, et al.
Published: (2018) -
Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations
by: Rachel K. Cason, et al.
Published: (2022) -
Genetic risk variants for childhood nephrotic syndrome and corticosteroid response
by: Rachel K. Cason, et al.
Published: (2023) -
Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An Update
by: Brandon M. Lane, et al.
Published: (2019) -
An Update on Glomerulopathies Etiology and Pathogenesis
Published: (2011)