Related Experiment Video
Updated: Apr 14, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Unusual Glomerular Abnormalities in a Patient With Combined COL4A5-NPHS1 Variants
Abdelrahman Alwan1, Carol Vincent2, Dmitry Lyalin3
1Department of Pathology, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, NC.
Combined genetic variants in collagen IV alpha 5 (COL4A5) and nephrin (NPHS1) genes cause a rare kidney disorder with unusual glomerular malformations in children. This finding highlights the importance of genetic analysis for diagnosing complex renal diseases.
Area of Science:
- Nephrology
- Genetics
- Molecular Biology
Background:
- Pathogenic variants in COL4A5 cause X-linked Alport syndrome, affecting the glomerular basement membrane (GBM).
- Pathogenic NPHS1 variants cause autosomal recessive childhood nephrotic syndrome, impacting the podocyte slit diaphragm.
More Related Videos
Related Concept Videos
Renal Corpuscle
Glomerulus: Structure and Function
The glomerulus is a tiny, intricate network of capillaries located at the beginning of the nephron. It's enveloped by the Bowman's capsule and receives its blood supply from an afferent arteriole, which divides into numerous...
Nephrotic Syndrome I : Introduction
Nephrons
Renal Tubule and Collecting Duct
Proximal Convoluted Tubule (PCT):
The PCT is the initial segment of the renal tubule, extending from the Bowman's capsule that encloses the glomerulus. Its convoluted structure and microvilli-lined cells increase the surface area for reabsorption. The PCT reabsorbs glucose, amino acids, sodium, and water from the filtrate, ensuring essential...
Nephrotic Syndrome II : Assessment and Medical Management
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:

