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

Risk of Atypical HUS Among Family Members of Patients Carrying Complement Regulatory Gene Abnormality

25 Mar 2021

Abstract excerpt

INTRODUCTION: Atypical hemolytic uremic syndrome (aHUS) is mainly due to complement regulatory gene abnormalities with a dominant pattern but incomplete penetrance. Thus, healthy carriers can be identified in any family of aHUS patients, but it is unpredictable if they will eventually develop aHUS. METHODS: Patients are screened for 10 complement regulatory gene abnormalities and once a genetic alteration is...

Read the complete abstract on PubMed

Topics

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

Share to Blood groups and transfusion
Share to Complement system in diseases
Share to Escherichia coli research studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34169201
DOI: 10.1016/j.ekir.2021.03.885

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Risk of Atypical HUS Among Family Members of Patients Carrying Complement Regulatory Gene AbnormalityPMID 34169201Read ↗

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

Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.Semantic proximity Read ↗

Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestations.Semantic proximity Read ↗

Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

The genetics of atypical hemolytic uremic syndromeSemantic proximity Read ↗

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.Semantic proximity Read ↗

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.Semantic proximity Read ↗

Genetics of atypical hemolytic uremic syndrome (aHUS).Semantic proximity Read ↗

Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study.Semantic proximity Read ↗

Genetics and complement in atypical HUS.Semantic proximity Read ↗

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