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

A complementary component to atypical haemolytic uraemic syndrome.

BMJ case reports - 18 Jun 2013

Gandhi Vanita, Burns Aine, Goodship Timothy

Abstract excerpt

We describe a case of a 22-year-old man who presented with clinical features of atypical haemolytic uraemic syndrome and in whom genetic analysis of complement regulatory proteins demonstrated a CD46 mutation. He was treated with plasma exchange, intermittent haemodialysis and blood transfusions. At 6-month follow-up his haematological parameters and renal function showed complete resolution, and he experienced...

Read the complete abstract on PubMed

Topics

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

Share to Atypical Hemolytic Uremic Syndrome
Share to Complement System Proteins
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemolytic-Uremic Syndrome

Share to Immunoglobulins, Intravenous

Share to Methylprednisolone

Share to Treatment Outcome

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 23780777
DOI: 10.1136/bcr-2013-010214
PMCID: PMC3702985

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A complementary component to atypical haemolytic uraemic syndrome.PMID 23780777Read ↗

Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome.Semantic proximity Read ↗

Protein-losing enteropathy as a new phenotype in atypical hemolytic uremic syndrome caused by CD46 gene mutation.Semantic proximity Read ↗

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome.Semantic proximity Read ↗

Complement dysfunction in hemolytic uremic syndrome.Semantic proximity Read ↗

Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to a CD46 mutation in the setting of SMARCAL1-mediated inherited kidney disease.Semantic proximity Read ↗

Haemolytic uraemic syndrome.Semantic proximity Read ↗

Complement therapy in atypical haemolytic uraemic syndrome (aHUS)Semantic proximity Read ↗

A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndromeSemantic proximity Read ↗

Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes.Semantic proximity Read ↗

Identification of a new CD46 gene mutation site in a family with atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Rapid recovery of membrane cofactor protein (MCP; CD46) associated atypical haemolytic uraemic syndrome with plasma exchange.Semantic proximity Read ↗

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