Article

Urine Microscopy Revealing a Metabolic Disorder: a Case Report

2026-01-12

Abstract excerpt

<title>Abstract</title> <p> <bold>Background</bold> Primary hyperoxaluria type 3 is a rare autosomal recessive disorder caused by HOGA1 mutations, leading to recurrent calcium oxalate nephrolithiasis. Diagnosis is often delayed, and 24-hour urine oxalate measurements can be unreliable in patients with normal kidney function. Urine microscopy can detect high-density calcium oxalate monohydrate crystals, providin...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: a2224745-65b2-53af-bafd-21eb54be857a
DOI: 10.21203/rs.3.rs-8468051/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Urine Microscopy Revealing a Metabolic Disorder: a Case ReportDOI 10.21203/rs.3.rs-8468051/v1Read

Normative urinary excretion parameters for early identification of primary hyperoxaluria or other kidney stone associated diseases in infants < 8 weeks of lifeSemantic proximity Read

Late diagnosis of primary hyperoxaluria type III.Semantic proximity Read

Composite Phenotype: Recurrent Nephrolithiasis and Chronic Kidney Disease in an Adult with Biallelic <italic>SLC34A3</italic> and Monoallelic <italic>SLC3A1</italic> Pathogenic Variants - Who Is "The Culprit"?Semantic proximity Read

Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2.Semantic proximity Read

An Update on Evaluation and Management in Cystinuria.Semantic proximity Read

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine.Semantic proximity Read

Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.Semantic proximity Read

Metabolic and Genetic Evaluation in Children with Nephrolithiasis.Semantic proximity Read

When to suspect a genetic disorder in a patient with renal stones, and why.Semantic proximity Read

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.Semantic proximity Read

[Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].Semantic proximity Read

Case Report: A Multisystem Mystery: Unraveling HNF1β-Associated Glomerulocystic Disease in a 30-year-old FemaleSemantic proximity Read