Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Coexistence of Fabry disease with IgM nephropathy

1 Oct 2019

Abstract excerpt

RATIONALE: Coexistence of Fabry disease and IgM nephropathy is rare. The varying severity and unapparent clinical manifestation of Fabry disease makes it difficult to recognize when coexisting with another more prevalent cause of nephropathy requiring electron microscopy and genetic testing to confirm their coexistence. PATIENT CONCERNS: A 54-year-old female presented with proteinuria without any clinical signs...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amyloidosis: Diagnosis, Treatment, Outcomes
Share to Lysosomal Storage Disorders Research
Share to Renal Diseases and Glomerulopathies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 31593141
DOI: 10.1097/md.0000000000017566

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Coexistence of Fabry disease with IgM nephropathyPMID 31593141Read ↗

Diagnosing Fabry nephropathy: the challenge of multiple kidney disease.Semantic proximity Read ↗

Coexistence of Fabry Disease and Membranous Nephropathy: A Case Report.Semantic proximity Read ↗

Fabry Disease with Genetic Variants of Unknown Significance and Concomitant Immunoglobulin A Nephropathy.Semantic proximity Read ↗

Primary membranous nephropathy combined with ALECT-2 renal amyloidosis：a case reportSemantic proximity Read ↗

Case Report: The tree that hides the forest, a case of renal ANCA vasculitis concurrent with Fabry nephropathy.Semantic proximity Read ↗

Case Report: The tree that hides the forest, a case of renal ANCA vasculitis concurrent with Fabry nephropathy.Semantic proximity Read ↗

Alport syndrome misdiagnosed with IgA nephropathy from familial history: a case report and brief reviewSemantic proximity Read ↗

A Case Study of Fabry Nephropathy and Its Progression: The First Reported Case in MalaysiaSemantic proximity Read ↗

Simultaneous multicystic kidney and Anderson-Fabry disease: 2 separate entities or same side of the coin.Semantic proximity Read ↗

Mechanisms of Primary Membranous NephropathySemantic proximity Read ↗

Chronic kidney disease and an uncertain diagnosis of Fabry disease: approach to a correct diagnosis.Semantic proximity Read ↗

A Classical Phenotype of Fabry Disease with Novel Mutation Found by Kidney Biopsy, A Case Report.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.