Related Experiment Video
Updated: Jul 25, 2025

Estimation of Urinary Nanocrystals in Humans using Calcium Fluorophore Labeling and Nanoparticle Tracking Analysis
Published on: February 9, 2021
Cystinuria: urine sediment as a diagnostic test
María Pierna1, Mohamed Abdelgabar2, Raquel Fernández-Rivas3
1Department of Clinical Analyses, Hospital de Mérida, Polígono Nueva Ciudad s/n, 06800, Mérida, Badajoz, Spain.
Urinary sediment analysis is crucial for diagnosing conditions like cystinuria, even in older adults without prior history. Microscopic examination of urine sediment aids in identifying genetic diseases presenting as renal colic.
Area of Science:
- Clinical Laboratory Diagnostics
- Urology
- Medical Genetics
Background:
- Urinary sediment analysis is a key diagnostic tool in clinical laboratories.
- Standardized protocols for routine microscopic urinary sediment examination are essential.
- Accurate interpretation of urinary crystals is vital for disease identification.
Observation:
- An elderly male presented with acute left iliac fossa pain.
- Urinalysis revealed proteinuria and hematuria.
- Urinary sediment analysis identified abundant hexagonal crystals, characteristic of cystine.
Findings:
- The case confirmed cystinuria, a genetic disorder, diagnosed via urinary sediment microscopy.
- Amino acid analysis corroborated the presence of elevated cystine levels.
- This diagnosis was made in an elderly patient with no prior history, highlighting atypical presentation.
Implications:
- This case underscores the diagnostic value of routine urinary sediment examination.
- It demonstrates the potential for diagnosing genetic disorders like cystinuria in later life.
- Highlights the need for robust laboratory protocols for microscopic urinalysis.
Related Concept Videos
Urinary Tract Calculi I: Introduction
Urologic Endoscopic Procedure: Cystoscopic Examination
Urine Studies I: Urinalysis
Urine Studies II: Urine Culture and Sensitivity Test
Urinary Tract Calculi III: Medical Management
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...

